Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases
出版年份 2011 全文链接
标题
Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases
作者
关键词
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出版物
PLoS Genetics
Volume 7, Issue 10, Pages e1002325
出版商
Public Library of Science (PLoS)
发表日期
2011-11-02
DOI
10.1371/journal.pgen.1002325
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