SCOPUS 정보 검색 플랫폼

Volumn 1271, Issue 1, 1995, Pages 135-140

Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotype

(8) Morgan Hughes, John A a Sweeney, Mary G a Cooper, J Mark b Hammans, Simon R a Brockington, Martin a Schapira, Anthony H V a,b Harding, Anita E a Clark, John B a

a UNIVERSITY COLLEGE LONDON (United Kingdom)

b ROYAL FREE HOSPITAL (United Kingdom)

Author keywords

MELAS phenotype; Mitochondrion; mtDNA disease

Indexed keywords

MITOCHONDRIAL DNA;

ADULT; AGED; CLINICAL ARTICLE; CONFERENCE PAPER; ENCEPHALOMYOPATHY; FEMALE; GENOTYPE; HUMAN; LACTIC ACIDOSIS; MALE; MELAS SYNDROME; OPHTHALMOPLEGIA; PHENOTYPE; PRIORITY JOURNAL; STROKE;

ADOLESCENT; ADULT; AGE OF ONSET; BIOPSY; CHILD; CYTOCHROME B GROUP; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT COMPLEX III; ELECTRON TRANSPORT COMPLEX IV; FEMALE; GENOTYPE; HUMANS; MALE; MELAS SYNDROME; MIDDLE AGED; MITOCHONDRIAL ENCEPHALOMYOPATHIES; MUSCLE, SKELETAL; NAD(P)H DEHYDROGENASE (QUINONE); PHENOTYPE; POINT MUTATION; RNA, TRANSFER, LEU;

ATAXIA;

EID: 0029029469 PISSN: 09254439 EISSN: None Source Type: Journal
DOI: 10.1016/0925-4439(95)00020-5 Document Type: Article

Times cited : (90)

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