The A985 to G mutation of the medium-chain acyl-CoA dehydrogenase gene and sudden infant death syndrome in Normandy

Acta Paediatrica, International Journal of Paediatrics

Volumn 85, Issue 2, 1996, Pages 145-147

  Lecoq, I ^a   Mallet, E ^b   Bonte, J B ^a   Travert, G ^a  

^a CAEN UNIVERSITY HOSPITAL   (France)

^b HÔPITAL CHARLES NICOLLE   (France)

Author keywords

G985 mutation; Genetic screening; Medium chain acyl CoA dehydrogenase deficiency; Sudden infant death syndrome

Indexed keywords

MEDIUM CHAIN ACYL COENZYME A DEHYDROGENASE;

ARTICLE; CONTROLLED STUDY; ENZYME DEFICIENCY; EPIDEMIOLOGY; GENE MUTATION; GENETIC SCREENING; GEOGRAPHY; HETEROZYGOSITY; HUMAN; INBORN ERROR OF METABOLISM; INCIDENCE; NEWBORN; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SUDDEN INFANT DEATH SYNDROME;

EID: 0030062643     PISSN: 08035253     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1651-2227.1996.tb13980.x     Document Type: Article

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