Functional characterisation of mitochondrial tRNA(Tyr) mutation (5877-->GA) associated with familial chronic progressive external ophthalmoplegia.

作者信息

Sahashi K, Yoneda M, Ohno K, Tanaka M, Ibi T, Sahashi K

出版信息

J Med Genet. 2001 Oct;38(10):703-5. doi: 10.1136/jmg.38.10.703.

DOI:10.1136/jmg.38.10.703

PMID:11594340

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1734734/

Abstract

摘要

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