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1471-2350-15-36
1471-2350-15-36
http://dx.doi.org/10.1186/1471-2350-15-36
Compound heterozygous mutations in glycyl-tRNA synthetase are a proposed cause of systemic mitochondrial disease.
P356
Q31154625-6347845F-C779-405B-BC6C-306A97961A6F
P356
1471-2350-15-36
http://dx.doi.org/10.1186/1471-2350-15-36