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The spectrum of mutations of the aspartoacylase gene in Canavan disease in non-Jewish patients
British Library Online Contents | 1999| -
Sustained oral lysine supplementation in ornithine delta-aminotransferase deficiency
British Library Online Contents | 2001| -
-Ketothiolase (2-methylacetoacetyl-coenzyme A thiolase) deficiency: identification of two patients in Israel
British Library Online Contents | 1996| -
3-methylglutaconic Aciduria in the Iraqi-Jewish 'Optic Atrophy Plus' (Costeff) Syndrome
British Library Online Contents | 1994| -
Prenatal detection of Canavan disease (aspartoacylase deficiency) by DNA analysis
British Library Online Contents | 1994| -
Protracted Clinical Course for Patients with Canavan Disease
British Library Online Contents | 1993|
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