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Journal of Inherited Metabolic Disease

Volumn 25, Issue 3, 2002, Pages 207-214

Primary and secondary defects of the mitochondrial respiratory chain

(1) Schapira, A H V a

a ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME C OXIDASE; FRATAXIN; FREE RADICAL; IRON; MITOCHONDRIAL DNA; NITRIC OXIDE; PEROXYNITRITE; PROTEIN; RIBOSOME RNA; TRANSFER RNA;

AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; CELL METABOLISM; CONTROLLED STUDY; DIABETES MELLITUS; DISEASE SEVERITY; ENCEPHALOMYOPATHY; ENZYME DEFICIENCY; FRIEDREICH ATAXIA; GENE MUTATION; GENE REARRANGEMENT; GENETIC VARIABILITY; GENOTYPE PHENOTYPE CORRELATION; HEARING IMPAIRMENT; HOMEOSTASIS; HUMAN; HUNTINGTON CHOREA; LEIGH DISEASE; MITOCHONDRION; MOTOR NEURON DISEASE; ONSET AGE; OPHTHALMOPLEGIA; OXIDATIVE PHOSPHORYLATION; PHENOTYPE; POINT MUTATION; PREDICTION; PROTEIN ASSEMBLY; RESPIRATORY CHAIN; RESPIRATORY FUNCTION; WILSON DISEASE; ANIMAL; BIOSYNTHESIS; DEGENERATIVE DISEASE; ELECTRON TRANSPORT; GENETICS; METABOLISM; MUTATION; REVIEW;

ANIMAL; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT; HUMAN; MITOCHONDRIA; MUTATION; NEURODEGENERATIVE DISEASES; RNA, TRANSFER; ANIMALS; HUMANS;

EID: 0035990290 PISSN: 01418955 EISSN: None Source Type: Journal
DOI: 10.1023/A:1015629912477 Document Type: Article

Times cited : (51)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.