SPG11 mutations are common in familial cases of complicated hereditary spastic paraplegia

出版年份 2008 全文链接

标题

作者

关键词

出版物

Volume 70, Issue Issue 16, Part 2, Pages 1384-1389

出版商

Ovid Technologies (Wolters Kluwer Health)

发表日期

2008-03-13

DOI

10.1212/01.wnl.0000294327.66106.3d

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