Skip to main content
Journal of Medical Genetics logoLink to Journal of Medical Genetics
letter
. 2001 Oct;38(10):703–705. doi: 10.1136/jmg.38.10.703

Functional characterisation of mitochondrial tRNATyr mutation (5877G→A) associated with familial chronic progressive external ophthalmoplegia

K Sahashi, M Yoneda, K Ohno, M Tanaka, T Ibi, K Sahashi
PMCID: PMC1734734  PMID: 11594340

Full Text

The Full Text of this article is available as a PDF (136.8 KB).


Articles from Journal of Medical Genetics are provided here courtesy of BMJ Publishing Group

RESOURCES