about
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Mutant NDUFV2 subunit of mitochondrial complex I causes early onset hypertrophic cardiomyopathy and encephalopathyTMEM126A, encoding a mitochondrial protein, is mutated in autosomal-recessive nonsyndromic optic atrophyCABC1 gene mutations cause ubiquinone deficiency with cerebellar ataxia and seizuresPrenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disordersMitochondrial activities in human cultured skin fibroblasts contaminated by Mycoplasma hyorhinisMitochondrial cytochrome c oxidase deficiencyGenotyping microsatellite DNA markers at putative disease loci in inbred/multiplex families with respiratory chain complex I deficiency allows rapid identification of a novel nonsense mutation (IVS1nt -1) in the NDUFS4 gene in Leigh syndromeMutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletionNuclear outsourcing of RNA interference components to human mitochondria
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Dominique Chrétien
@ast
Dominique Chrétien
@en
Dominique Chrétien
@es
Dominique Chrétien
@nl
Dominique Chrétien
@sl
type
label
Dominique Chrétien
@ast
Dominique Chrétien
@en
Dominique Chrétien
@es
Dominique Chrétien
@nl
Dominique Chrétien
@sl
altLabel
Dominique Chretien
@en
Dominique Chretien
@nl
prefLabel
Dominique Chrétien
@ast
Dominique Chrétien
@en
Dominique Chrétien
@es
Dominique Chrétien
@nl
Dominique Chrétien
@sl