Novel mtDNA mutations and oxidative phosphorylation dysfunction in Russian LHON families

Human Genetics

Volumn 109, Issue 1, 2001, Pages 33-39

  Brown, M D ^a   Zhadanov, S ^a   Allen, J C ^a   Hosseini, S ^a   Newman, N J ^a   Atamonov, V V ^a   Mikhailovskaya, I E ^a   Sukernik, R I ^a   Wallace, D C ^a  

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COAT PROTEIN COMPLEX I; MITOCHONDRIAL DNA; POLYPEPTIDE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE;

ADULT; ARTICLE; BASE PAIRING; BIOCHEMISTRY; CELL RESPIRATION; CENTRAL SCOTOMA; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE TRANSMISSION; ENZYME DEFECT; ENZYME SUBSTRATE COMPLEX; EUROPE; FAMILY; FEMALE; GENE EXPRESSION; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC CODE; HEREDITARY OPTIC ATROPHY; HUMAN; HUMAN CELL; HYBRID CELL; LYMPHOBLAST; MALE; MEDICAL LITERATURE; MITOCHONDRIAL RESPIRATION; NORTH AMERICA; NUCLEOTIDE SEQUENCE; OXIDATIVE PHOSPHORYLATION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; RUSSIAN FEDERATION; SEQUENCE ANALYSIS;

ADOLESCENT; ADULT; CASE-CONTROL STUDIES; CELL LINE; CHILD; DNA MUTATIONAL ANALYSIS; DNA, MITOCHONDRIAL; FEMALE; HUMANS; MALE; MUTATION; OPTIC ATROPHIES, HEREDITARY; OXIDATIVE PHOSPHORYLATION; PEDIGREE; RUSSIA;

EID: 0034904756     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390100538     Document Type: Article

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