Parkin disease: a phenotypic study of a large case series
Parkin disease: a phenotypic study of a large case series
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DOI：
10.1093/brain/awg142
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发表时间：
2003-06-01
期刊：
影响因子：
14.5
通讯作者：
Quinn, N
中科院分区：
文献类型：
--
作者：
Khan, NL;Graham, E;Quinn, N
Parkin 基因 PARK2 突变是家族性帕金森症以及发病年龄不同的孤立病例的常见原因
Mutations in the parkin gene, PARK2, are a common cause of parkinsonism in familial as well as isolated cases with an age of onset