Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial M-Aaa Proteases
PLoS Genetics - United States
doi 10.1371/journal.pgen.1002325
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Date
October 13, 2011
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Public Library of Science (PLoS)