Adult-onset arginase deficiency

Journal of Inherited Metabolic Disease

Volumn 21, Issue 6, 1998, Pages 677-678

  Cowley, D M ^a,c   Bowling, F G ^a,c   McGiil, J J ^a   Van Dongen, J ^a   Morris, D ^b  

^a MATER HOSPITAL   (Australia)

^b QUEENSLAND HEALTH   (Australia)

^c Mater Hospitals ^*  (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ARGINASE;

ADULT; ARTICLE; CASE REPORT; ENZYME DEFICIENCY; FEMALE; HEPATOMEGALY; HUMAN; ONSET AGE; SPASTICITY;

ADOLESCENT; AMINO ACID METABOLISM, INBORN ERRORS; ARGINASE; ARGININE; FEMALE; HUMANS;

EID: 0031720666     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005492819527     Document Type: Article

References (3)

1. Jenkinson CP, Grody WW, Cederbaum SD (1996) Comparative properties of arginases. Comp Biochem Physiol 114B: 107-132.
2. Prasad AN, Breen JC, Ampola MG, Rosman P (1997) Argininaemia: a treatable genetic cause of progressive spastic diplegia simulating cerebral palsy. Case reports and literature review. J Child Neurol 12: 301-309.
3. Vockley JG, Goodman BK, Tabor PE et al (1996) Loss of function mutation in conserved regions of the human arginase I gene. Biochem Mol Med 59: 44-51.