Clinical outcomes in long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency [2] (multiple letters)

Journal of Pediatrics

Volumn 131, Issue 6, 1997, Pages 938-

  Morris, A A M ^a   Clayton, P T ^a   Surtees, R A H ^a   Leonard, J V ^a   Tyni, T ^a   Pibko, H ^a  

^a ROYAL VICTORIA INFIRMARY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

3 HYDROXYACYL COENZYME A DEHYDROGENASE;

BRAIN DISEASE; CARDIOMYOPATHY; CHILD; CLINICAL ARTICLE; DIET THERAPY; ENZYME DEFICIENCY; FATTY ACID OXIDATION; HUMAN; HYPOGLYCEMIA; LETTER; PRIORITY JOURNAL; RHABDOMYOLYSIS;

EID: 0031444649     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(97)70052-0     Document Type: Letter

References (3)

1. T Tyni A Palotie L Viinikka L Valanne MK Salo U von Dobeln Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency with the G1528C mutation: clinical presentation of 13 patients J Pediatr 130 1997 67 76
2. R Pons M Roig E Riudor A Ribes P Briones L Ortigosa The clinical spectrum of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency Pediatr Neurol 14 1996 236 243
3. L IJlst J Ruiter J Hoovers M Jakobs R Wanders Common missense mutation G1528C in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency J Clin Invest 98 1996 1028 1033