Publication | Closed Access
Infantile cardiomyopathy caused by the T14709C mutation in the mitochondrial tRNA glutamic acid gene
16
Citations
15
References
2007
Year
CardiomyopathyMitochondrial FunctionGeneticsInherited Metabolic DiseasePhysiologyMolecular BiologyInfantile CardiomyopathyMitochondrial MedicineMolecular GeneticsT14709c MutationMedicine
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