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[期刊论文] 作者:Hongfeng Zhang,Yujuan Hong,Weijie Yang,Ruimin Wang,Ting Yao,Jian Wang,Ke Liu,Huilong Yuan,Chaoqun Xu,, 来源:国家科学评论:英文版 年份:2021
Loss-of-function mutations in sorting nexin 14(SNX14)cause autosomal recessive spinocerebellar ataxia 20,which is a form of early-onset cerebellar ataxia that lacks molecular mechanisms and mouse models.We generated Snx14-deficient mouse mo......
[期刊论文] 作者:Hongfeng Zhang,Yujuan Hong,Weijie Yang,Ruimin Wang,Ting Yao,Jian Wang,Ke Liu,Huilong Yuan,Chaoqun Xu,, 来源:国家科学评论(英文版) 年份:2021
Loss-of-function mutations in sorting nexin 14(SNX14)cause autosomal recessive spinocerebellar ataxia 20,which is a form of early-onset cerebellar ataxia that lacks molecular mechanisms and mouse models.We generated Snx1 4-deficient mouse m......
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