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Article

Benign reversible course in infants manifesting clinicopathological features of fatal mitochondrial myopathy due to m.14674 T>C mt-tRNAGlu mutation.

QJM : monthly journal of the Association of Physicians - 1 Oct 2013

Chen T-H, Tu Y-F, Goto Y-I, Jong Y-J

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Share to Biopsy
Share to Cytochrome-c Oxidase Deficiency
Share to Diagnosis, Differential
Share to DNA, Mitochondrial

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Infant, Newborn

Share to Intensive Care Units, Neonatal

Share to Mitochondrial Myopathies

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Identifiers

PMID: 23842486
DOI: 10.1093/qjmed/hct151

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Benign reversible course in infants manifesting clinicopathological features of fatal mitochondrial myopathy due to m.14674 T>C mt-tRNAGlu mutation.PMID 23842486Read ↗

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