Very long chain acyl coenzyme A dehydrogenase deficiency in a 5-month- old Korean boy: Identification of a novel mutation

Journal of Pediatrics

Volumn 135, Issue 2 I, 1999, Pages 250-253

  Hahn, S H ^a   Lee, E H ^a   Jung, J W ^a   Hong, C H ^a   Yoon, H R ^a   Rinaldo, P ^a   Sims, H ^a   Gibson, B ^a   Strauss, A W ^a  

^a Ajou University School of Medicine   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

ACYL COENZYME A DEHYDROGENASE; VERY LONG CHAIN FATTY ACID;

ARTICLE; ASIAN; CASE REPORT; CONTROLLED STUDY; ENZYME DEFICIENCY; GENE DELETION; GENE MUTATION; GENETIC HETEROGENEITY; HETEROZYGOTE; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; INFANT; KOREA; LETHARGY; MALE; MOLECULAR GENETICS; PRIORITY JOURNAL;

EID: 0033497370     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(99)70030-2     Document Type: Article

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