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Paper Details

Genetic diversity of NDUFV1-dependent mitochondrial complex I deficiency.
Eur J Hum Genet
15
2018
Arg386Cys, Autosomal recessive mitochondrial complex I deficiency, FMN, Leigh Syndrome, MCID, NADH, NADH dehydrogenase, NDUFV1, NDUFV1-dependent mitochondrial complex I deficiency, Phe373Ser), c.1118T, c.1156C, complex I, developmental disorders, encephalopathies, inherited risk variants, mitochondrial, mitochondrial complex I, myopathies, population
Author NameAffiliation
Xuhong CaoHoward Hughes Medical Institute, Michigan Center for Translational Pathology, University of Michigan ann arbor
Xuhong CaoUniversity of Michigan Medical School ann arbor
Arul M ChinnaiyanHoward Hughes Medical Institute, Michigan Center for Translational Pathology, University of Michigan ann arbor
Arul M ChinnaiyanUniversity of Michigan Medical School ann arbor
Arul M ChinnaiyanHoward Hughes Medical Institute, Michigan Center for Translational Pathology, University of Michigan ann arbor
Arul M ChinnaiyanUniversity of Michigan Medical School ann arbor
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