PNKP Mutations Identified by Whole-Exome Sequencing in a Norwegian Patient with Sporadic Ataxia and Edema

出版年份 2016 全文链接

标题

作者

关键词

Ataxia, Oculomotor apraxia, Edema, Hypoalbuminemia, AOA4

出版物

Volume 16, Issue 1, Pages 272-275

出版商

Springer Nature

发表日期

2016-05-10

DOI

10.1007/s12311-016-0784-y

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