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掌腱膜挛缩症
掌腱膜挛缩症
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掌腱膜挛缩症
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想问问这个是什么病症？网上搜看不太懂，而且亚洲人发病率低一些
俊逸的TMTC1基因
• 最后回复
wendy0425
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2019-12-24 15:24
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掌腱膜挛缩症
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相关基因
DUXA
位点：RS11672517
EPDR1
位点：RS16879765
位点：RS2598107
WNT2
位点：RS4730775
EIF3E
位点：RS611744
DDR2
位点：RS17433710
ZC3H12D
位点：RS394563
EBF2
位点：RS10866846
BOP1
位点：RS7838717
MMP14
位点：RS1042704
ATL1
位点：RS1032466
NEDD4
位点：RS1509406
ITGA11
位点：RS2306022
CHST6
位点：RS977987
RAB31
位点：RS9951109
A genome-wide association study of Dupuytren disease reveals 17 additional variants implicated in fibrosis
Wnt signaling and Dupuytren's disease.
Wnt signaling and Dupuytren's disease.
A genome-wide association study of Dupuytren disease reveals 17 additional variants implicated in fibrosis
A genome-wide association study of Dupuytren disease reveals 17 additional variants implicated in fibrosis
A genome-wide association study of Dupuytren disease reveals 17 additional variants implicated in fibrosis
A genome-wide association study of Dupuytren disease reveals 17 additional variants implicated in fibrosis
A genome-wide association study of Dupuytren disease reveals 17 additional variants implicated in fibrosis
A genome-wide association study of Dupuytren disease reveals 17 additional variants implicated in fibrosis
A genome-wide association study of Dupuytren disease reveals 17 additional variants implicated in fibrosis
A genome-wide association study of Dupuytren disease reveals 17 additional variants implicated in fibrosis
A genome-wide association study of Dupuytren disease reveals 17 additional variants implicated in fibrosis
A genome-wide association study of Dupuytren disease reveals 17 additional variants implicated in fibrosis
A genome-wide association study of Dupuytren disease reveals 17 additional variants implicated in fibrosis
A genome-wide association study of Dupuytren disease reveals 17 additional variants implicated in fibrosis
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