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American Journal of Human Genetics

Volumn 68, Issue 1, 2001, Pages 238-240

Decrease of 3243 A→G mtDNA mutation from blood in MELAS syndrome: A longitudinal study

(4) Rahman, S a Poulton, J b Marchington, D b Suomalainen, A c

a UNIVERSITY COLLEGE LONDON (United Kingdom)

b UNIVERSITY OF OXFORD (United Kingdom)

c NATIONAL PUBLIC HEALTH INSTITUTE (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ADOLESCENT; ADULT; AMINO ACID SUBSTITUTION; ARTICLE; BIRTH; BLOOD SAMPLING; CLINICAL ARTICLE; GENE MUTATION; HUMAN; MELAS SYNDROME; PRIORITY JOURNAL; SCHOOL CHILD; SEQUENCE ANALYSIS; BLOOD; CHILD; DNA SEQUENCE; GENETICS; LONGITUDINAL STUDY; MUTATION; NEWBORN; NUCLEOTIDE SEQUENCE; TIME;

ADOLESCENT; ADULT; CHILD; DNA MUTATIONAL ANALYSIS; DNA, MITOCHONDRIAL; HUMANS; INFANT, NEWBORN; LONGITUDINAL STUDIES; MELAS SYNDROME; MUTATION; SEQUENCE ANALYSIS, DNA; TIME FACTORS;

EID: 0034746790 PISSN: 00029297 EISSN: None Source Type: Journal
DOI: 10.1086/316930 Document Type: Article

Times cited : (205)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.