Maternally inherited diabetes and deafness with cerebellar ataxia: a new clinical phenotype associated with the mitochondrial DNA 3243 mutation.

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作者信息

Arai M, Ohshima S

出版信息

J Neurol. 1997 Jul;244(7):468-9. doi: 10.1007/s004150050126.

DOI:10.1007/s004150050126

PMID:9266470

Abstract

摘要

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引用本文的文献

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