Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness.
Manouvrier, S, Rotig, A, Hannebique, G, Gheerbrandt, J D, Royer-Legrain, G, Munnich, A, Parent, M, Grunfeld, J P, Largilliere, C, Lombes, AVolume:
32
Language:
english
Journal:
Journal of Medical Genetics
DOI:
10.1136/jmg.32.8.654
Date:
August, 1995
File:
PDF, 520 KB
english, 1995