Mutations in KCND3 cause spinocerebellar ataxia type 22.
KCND3 基因突变会导致 22 型脊髓小脑性共济失调
期刊:Annals of Neurology
影响因子:7.7
doi:10.1002/ana.23701
Lee Yi-Chung, Durr Alexandra, Majczenko Karen, Huang Yen-Hua, Liu Yu-Chao, Lien Cheng-Chang, Tsai Pei-Chien, Ichikawa Yaeko, Goto Jun, Monin Marie-Lorraine, Li Jun Z, Chung Ming-Yi, Mundwiller Emeline, Shakkottai Vikram, Liu Tze-Tze, Tesson Christelle, Lu Yi-Chun, Brice Alexis, Tsuji Shoji, Burmeister Margit, Stevanin Giovanni, Soong Bing-Wen