A genomewide linkage-disequilibrium scan localizes the Saguenay-Lac-Saint-Jean cytochrome oxidase deficiency to 2p16

American Journal of Human Genetics

Volumn 68, Issue 2, 2001, Pages 397-409

  Lee, Nana ^a,b   Daly, Mark J ^c   Delmonte, Terrye ^c   Lander, Eric S ^c,d   Xu, Fenghao ^a   Hudson, Thomas J ^c,e   Mitchell, Grant A ^f   Morin, Charles C ^g   Robinson, Brian H ^a,b   Rioux, John D ^c  

^a HOSPITAL FOR SICK CHILDREN RESEARCH INSTITUTE   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

^c WHITEHEAD INSTITUTE FOR BIOMEDICAL RESEARCH   (United States)

^d MASSACHUSETTS INSTITUTE OF TECHNOLOGY   (United States)

^e RESEARCH INSTITUTE OF THE MCGILL UNIVERSITY HEALTH CENTRE   (Canada)

^f UNIVERSITY OF MONTREAL   (Canada)

^g CHICOUTIMI HOSPITAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME C OXIDASE;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOMAL LOCALIZATION; CHROMOSOME 2P; CLINICAL ARTICLE; DNA SEQUENCE; ENZYME DEFICIENCY; FOUNDER EFFECT; GENE LINKAGE DISEQUILIBRIUM; GENE STRUCTURE; GENETIC SCREENING; GENOME; GENOTYPE; GROWTH RETARDATION; HUMAN; LACTIC ACIDOSIS; LEIGH DISEASE; MUSCLE HYPOTONIA; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

EID: 0035128063     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/318197     Document Type: Article

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