使用本網站需要啟用 JavaScript, 請啟用后刷新頁面獲得更好的體驗
亚洲精品午夜精品,日本二手网站,国产AⅤ爽AV久久久久成人社区,日本一二三区不收费av
<label id="ytfww"><center id="ytfww"></center></label>
<i id="ytfww"></i>
<p id="ytfww"></p>
登錄
注冊
首頁
個人居家檢測
臨床應用研究
科研合作項目
合作與服務
社區
純合片段分析
姓氏祖源
祖源平均臉
基因關系
基因保險助手
原始數據
使用 WeGene 需要啟用 Cookies, 請啟用后刷新頁面獲得更好的體驗
社區首頁
小組
帕金森
帕金森
發起討論
帕金森
7 個討論
只看精華帖
按熱門排序
按最新排序
帕金森27倍風險怎么辦。。
nniiuuly
? 最后回復
竹林深處
?
2024-09-03 18:26
2549
5
? 來自相關小組
帕金森比一般人患病風險高6.2倍，天吶，該怎么辦？
fanglongzong
? 最后回復
私奔的CSMD3基因
?
2019-07-03 17:22
3772
4
? 來自相關小組
我的帕金森風險是平均人群的21.8倍。。
買醉的NRG1基因
? 最后回復
chachq
?
2019-02-13 17:11
5813
12
? 來自相關小組
更新了，現在是0.62
樂觀的TUSC3基因
? 最后回復
樂觀的TUSC3基因
?
2018-09-01 11:06
2939
1
? 來自相關小組
查了原始數據，我的rs421016是GG，根據snpedia這個位點等于GG表示高雪氏病和>5倍的帕金森風險
jameszeng
? 最后回復
yaoxt
?
2016-12-31 22:25
4102
1
? 來自相關小組
帕金森風險是正常人的五倍還多，能做什么預防措施嗎？
聰明的SNX29基因
? 最后回復
yaoxt
?
2016-12-15 10:11
4023
3
? 來自相關小組
我父親和叔叔有帕金森，我想把我的更多數據貢獻給科學，有渠道嗎？
digitalboy
? 最后回復
cqnyfz
?
2015-11-19 09:37
4850
2
? 來自相關小組
發起討論
帕金森
7 個討論
相關基因
MCCC1
位點：RS10513789
位點：RS12637471
EIF4G1
位點：RS111290936
位點：RS112019125
位點：RS112176450
位點：RS113169049
位點：RS113388242
PHACTR2
位點：RS11155313
SREBF1
位點：RS11868035
RIT2
位點：RS12456492
SLC45A3
位點：RS16856139
SLC2A13
位點：RS1994090
NSF
位點：RS199533
SNCA
位點：RS2736990
位點：RS356203
LRRK2
位點：RS33949390
位點：RS34637584
位點：RS34778348
CRHR1-IT1
位點：RS393152
GBA
位點：RS421016
位點：RS76763715
CASC16
位點：RS4784227
FAM47E
位點：RS6812193
NUCKS1
位點：RS823128
LINGO1
位點：RS9652490
KCNIP3
位點：RS2042477
SCN2A
位點：RS353116
IP6K2
位點：RS12497850
SPTSSB
位點：RS1450522
TMEM175
位點：RS34311866
TRIM40
位點：RS9261484
SLC44A4
位點：RS9267659
GPNMB
位點：RS199351
BIN3
位點：RS2280104
ITGA8
位點：RS896435
GBF1
位點：RS10748818
IGSF9B
位點：RS3802920
HIP1R
位點：RS10847864
CCDC62
位點：RS11060180
GCH1
位點：RS11158026
NOD2
位點：RS6500328
MGC57346-CRHR1
位點：RS117615688
Web-Based Genome-Wide Association Study Identifies Two Novel Loci and a Substantial Genetic Component for Parkinson's Disease
Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease
Phactr2 and Parkinson's disease
Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease
Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease
Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease
Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease
Web-Based Genome-Wide Association Study Identifies Two Novel Loci and a Substantial Genetic Component for Parkinson’s Disease
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson’s disease
Web-Based Genome-Wide Association Study Identifies Two Novel Loci and a Substantial Genetic Component for Parkinson's Disease
Genome-Wide Association Study reveals genetic risk underlying Parkinson’s disease
Genome-Wide Association Study reveals genetic risk underlying Parkinson’s disease
LRRK2 R1628P increases risk of Parkinson’s disease: replication evidence
Web-Based Genome-Wide Association Study Identifies Two Novel Loci and a Substantial Genetic Component for Parkinson's Disease
Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database
Genome-Wide Association Study reveals genetic risk underlying Parkinson’s disease
Tsuji S, et al. Genetic heterogeneity in type 1 Gaucher disease: multiple genotypes in Ashkenazic and non-Ashkenazic individuals. 1988
Sidransky E, et al. Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease. 2009
Firon N, et al. Genotype assignment in Gaucher disease by selective amplification of the active glucocerebrosidase gene. 1990
Latham T, et al. Complex alleles of the acid beta-glucosidase gene in Gaucher disease. 1990
Wigderson M, et al. Characterization of mutations in Gaucher patients by cDNA cloning. 1989
Tsuji S, et al. A mutation in the human glucocerebrosidase gene in neuronopathic Gaucher's disease. 1987
A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci
Web-Based Genome-Wide Association Study Identifies Two Novel Loci and a Substantial Genetic Component for Parkinson’s Disease
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Genome-Wide Association Study reveals genetic risk underlying Parkinson’s disease
LINGO1 rs9652490 is associated with Essential Tremor and Parkinson Disease
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
查看參考文獻
首頁
個人基因檢測
臨床應用研究
科研合作項目
合作與服務
示例報告
下載 APP
社區
關于 WeGene
關于我們
媒體新聞
倫理委員會
隱私協議
加入我們
服務協議
價格保護
幫助中心
關于基因檢測
賬戶購買
樣本寄送
報告解讀
隱私安全
關于第三方數據
社區分享
開放平臺
申請成為開發者
開發文檔
客服微信公眾號
聯系我們
客服郵箱：
[email protected]
合作咨詢：
[email protected]
© 2025 WeGene. All Rights Reserved
深圳市市場監督管理局企業主體身份公示
|
粵ICP備15012185號
| 互聯網藥品信息服務資格證書:（粵）-非經營性-2023-0379
中文
English
<track id="ffr4e"></track>
<dfn id="ffr4e"></dfn>
主站蜘蛛池模板：
红桥区
|
永清县
|
拜泉县
|
乌拉特后旗
|
抚远县
|
改则县
|
惠州市
|
汉中市
|
板桥市
|
丰台区
|
襄垣县
|
张家口市
|
松桃
|
南安市
|
河源市
|
临桂县
|
南溪县
|
商丘市
|
大冶市
|
信宜市
|
沅江市
|
泰来县
|
长治县
|
嘉黎县
|
邹平县
|
交口县
|
长白
|
上饶市
|
会宁县
|
临夏市
|
梁平县
|
元阳县
|
屯门区
|
仙游县
|
平罗县
|
楚雄市
|
鄄城县
|
涿州市
|
南澳县
|
依兰县
|
丽江市
|
<center id="0ssjq"><em id="0ssjq"></em></center>
<pre id="0ssjq"><li id="0ssjq"><label id="0ssjq"></label></li></pre>
<bdo id="0ssjq"><dl id="0ssjq"></dl></bdo>
純合片段分析
姓氏祖源
祖源平均臉
基因關系
基因保險助手
原始數據
深圳市市場監督管理局企業主體身份公示
中文
English