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Published in 2019 at "Clinical Genetics"
DOI: 10.1111/cge.13496
Abstract: To the Editor: The variant m.3243A>G is one of the most frequent causes of mitochondrial dysfunction and is responsible for myopathy, encephalopathy, lactic acidosis and stroke-like episodes and other phenotypes. Its degree of heteroplasmy (H)…
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Keywords:
insights decrease;
quantitative insights;
decrease heteroplasmy;
age ... See more keywords