Lv6
2738 积分 2022-04-04 加入
SCA42 mutation analysis in a case series of Japanese patients with spinocerebellar ataxia
12小时前
已完结
A case of a novel CACNA1G mutation from a Chinese family with SCA42
12小时前
已完结
CACNA1G Causes Dominantly Inherited Myoclonus-Ataxia with Intellectual Disability: A Case Report
4天前
已完结