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Published in 2018 at "Human Molecular Genetics"
DOI: 10.1093/hmg/ddy247
Abstract: Abstract Complex I deficiency is a common cause of mitochondrial disease, resulting from mutations in genes encoding structural subunits, assembly factors or defects in mitochondrial gene expression. Advances in genetic diagnostics and sequencing have led…
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Keywords:
ind1;
yarrowia lipolytica;
model yarrowia;
yeast model ... See more keywords