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Volumn 26, Issue 1, 2011, Pages 12-20

Molecular-clinical correlation in a family with a novel heteroplasmic leigh syndrome missense mutation in the mitochondrial cytochrome c oxidase III gene

Author keywords

COXIII; Leigh syndrome; m.9478T>C; mitochondrial mutation

Indexed keywords

ALANINE; CYTOCHROME C OXIDASE; MITOCHONDRIAL CYTOCHROME C OXIDASE III; NUCLEOTIDE; UNCLASSIFIED DRUG; VALINE;

EID: 78651329718     PISSN: 08830738     EISSN: 17088283     Source Type: Journal    
DOI: 10.1177/0883073810371227     Document Type: Article
Times cited : (22)

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