Clinical phenotype in silico and biomedical analyses and intervention for an East Asian populationspecific c.370G>A p.G124S COQ4 mutation in a Chinese family with CoQ10 deficiencyassociated Leigh syndrome

Clinical phenotype, in silico and biomedical analyses, and intervention for an East Asian population-specific c.370G>A (p.G124S) COQ4 mutation in a Chinese family with CoQ10 deficiency-associated Leigh syndrome

10:57 EST 18 Jan 2019 | Nature Publishing

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