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帕金森
帕金森
發起討論
帕金森
7 個討論
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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
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<pre id="0ssjq"><li id="0ssjq"><label id="0ssjq"></label></li></pre>
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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