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[G14453A mutation in mitochondrial myopathy encephalomyopathy with lactic acidosis and stroke-like episodes].

Zhonghua yi xue za zhi - 25 Aug 2015

Zheng Xuefei, Zhang Yanchun, Zhang Ying, Pei Pei, Ma Yinan

Abstract excerpt

OBJECTIVE: To analyz mitochondrial DNA mutation in one case of mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS). METHODS: The patient, a 10-years-old boy,clinically diagnosed as MELAS. The clinical information was collected, and the normal mitochondrial mutations (such as A3243G, A8344G, T8993G/C, G13513A etc) were excluded. PCR-sequencing was used to analyz the...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 26711613

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