Late-onset holocarboxylase syethetase deficiency

Journal of Inherited Metabolic Disease

Volumn 19, Issue 6, 1996, Pages 739-742

  Glbson, K M ^a  

^a BAYLOR RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BIOTIN; CARBOXYLIC ACID;

ARTICLE; CASE REPORT; CHILD; ENZYME DEFICIENCY; FEMALE; HUMAN; ONSET AGE; PRESCHOOL CHILD; URINE;

BIOTIN; CARBON-NITROGEN LIGASES; FEMALE; HUMANS; INFANT; LIGASES;

EID: 0029852406     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1007/bf01799165     Document Type: Article

References (2)

1. l3C-propionate in vivo in patients with disorders of propionate metabolism. Pediatr Res 30: 15-22.
2. Dabbagh O, Brismar J, Gascon GG, Ozand PT (1994) The clinical spectrum of biotin-treatable encephalopathies in Saudi Arabia. Brain Dev 16(supplement): 72-80.