Fatal Infantile Mitochondrial Encephalomyopathy, Hypertrophic Cardiomyopathy and Optic Atrophy Associated With a homozygousOPA1mutation
Journal of Medical Genetics - United Kingdom
doi 10.1136/jmedgenet-2015-103361
Full Text
Open PDFAbstract
Available in full text
Categories
Date
November 11, 2015
Authors
Publisher
BMJ