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Compound heterozygous mutations in glycyl-tRNA synthetase are a proposed cause of systemic mitochondrial disease
McMillan, Hugh J, Schwartzentruber, Jeremy, Smith, Amanda, Lee, Suzie, Chakraborty, Pranesh, Bulman, Dennis E, Beaulieu, Chandree L, Majewski, Jacek, Boycott, Kym M, Geraghty, Michael TVolume:
15
Language:
english
Journal:
BMC Medical Genetics
DOI:
10.1186/1471-2350-15-36
Date:
December, 2014
File:
PDF, 398 KB
english, 2014