Carnitine-acylcarnitine translocase deficiency - a mild phenotype

Journal of Inherited Metabolic Disease

Volumn 20, Issue 5, 1997, Pages 714-715

  Olpin, S E ^a   Bonham, J R ^a   Downing, M ^a   Manning, N J ^a   Pollitt, R J ^a   Sharrard, M J ^a   Tanner, M S ^a  

^a SHEFFIELD CHILDREN S HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ACYLCARNITINE; CARNITINE; CARRIER PROTEIN;

ARTICLE; CASE REPORT; CHILD; ENZYME DEFICIENCY; HUMAN; MALE; PHENOTYPE; PRESCHOOL CHILD;

CARNITINE ACYLTRANSFERASES; HUMANS; INFANT; MALE; PHENOTYPE;

EID: 0030776297     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005343013873     Document Type: Article

References (3)