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帕金森
帕金森
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帕金森
7 个讨论
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帕金森27倍风险怎么办。。
nniiuuly
• 最后回复
竹林深处
•
2024-09-03 18:26
1957
5
• 来自相关小组
帕金森比一般人患病风险高6.2倍,天呐,该怎么办?
fanglongzong
• 最后回复
私奔的CSMD3基因
•
2019-07-03 17:22
3525
4
• 来自相关小组
我的帕金森风险是平均人群的21.8倍。。
买醉的NRG1基因
• 最后回复
chachq
•
2019-02-13 17:11
5575
12
• 来自相关小组
更新了,现在是0.62
乐观的TUSC3基因
• 最后回复
乐观的TUSC3基因
•
2018-09-01 11:06
2700
1
• 来自相关小组
查了原始数据,我的rs421016是GG,根据snpedia这个位点等于GG表示高雪氏病和>5倍的帕金森风险
jameszeng
• 最后回复
yaoxt
•
2016-12-31 22:25
3801
1
• 来自相关小组
帕金森风险是正常人的五倍还多,能做什么预防措施吗?
聪明的SNX29基因
• 最后回复
yaoxt
•
2016-12-15 10:11
3726
3
• 来自相关小组
我父亲和叔叔有帕金森,我想把我的更多数据贡献给科学,有渠道吗?
digitalboy
• 最后回复
cqnyfz
•
2015-11-19 09:37
4288
2
• 来自相关小组
发起讨论
帕金森
7 个讨论
相关基因
MCCC1
位点:RS10513789
位点:RS12637471
EIF4G1
位点:RS111290936
位点:RS112019125
位点:RS112176450
位点:RS113169049
位点:RS113388242
PHACTR2
位点:RS11155313
SREBF1
位点:RS11868035
RIT2
位点:RS12456492
SLC45A3
位点:RS16856139
SLC2A13
位点:RS1994090
NSF
位点:RS199533
SNCA
位点:RS2736990
位点:RS356203
LRRK2
位点:RS33949390
位点:RS34637584
位点:RS34778348
CRHR1-IT1
位点:RS393152
GBA
位点:RS421016
位点:RS76763715
CASC16
位点:RS4784227
FAM47E
位点:RS6812193
NUCKS1
位点:RS823128
LINGO1
位点:RS9652490
KCNIP3
位点:RS2042477
SCN2A
位点:RS353116
IP6K2
位点:RS12497850
SPTSSB
位点:RS1450522
TMEM175
位点:RS34311866
TRIM40
位点:RS9261484
SLC44A4
位点:RS9267659
GPNMB
位点:RS199351
BIN3
位点:RS2280104
ITGA8
位点:RS896435
GBF1
位点:RS10748818
IGSF9B
位点:RS3802920
HIP1R
位点:RS10847864
CCDC62
位点:RS11060180
GCH1
位点:RS11158026
NOD2
位点:RS6500328
MGC57346-CRHR1
位点:RS117615688
Web-Based Genome-Wide Association Study Identifies Two Novel Loci and a Substantial Genetic Component for Parkinson's Disease
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Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease
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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
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Genome-Wide Association Study reveals genetic risk underlying Parkinson’s disease
LINGO1 rs9652490 is associated with Essential Tremor and Parkinson Disease
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A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci
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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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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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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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Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
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