bibliographic entry 8003915 [be/8003915]
https://w3id.org/oc/corpus/be/8003915
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Kopajtich R, Nicholls TJ, Rorbach J, Metodiev MD, Freisinger P, Mandel H, et al (2014) Mutations in GTPBP3 Cause a Mitochondrial Translation Defect Associated with Hypertrophic Cardiomyopathy, Lactic Acidosis, and Encephalopathy. Am J Hum Genet 95: 708â720. doi: 10.1016/j.ajhg.2014.10.017 PMID: 25434004
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