Outcome of the First 3-Years of a DNA-Based Neonatal Screening Program for Glutaric Acidemia Type 1 in Manitoba and Northwestern Ontario, Canada-Reference-Cited by-同舟云学术

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Outcome of the First 3-Years of a DNA-Based Neonatal Screening Program for Glutaric Acidemia Type 1 in Manitoba and Northwestern Ontario, Canada

Published:2002-01 Issue:1 Volume:75 Page:70-78
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Greenberg C.R.,Prasad A.N.,Dilling L.A.,Thompson J.R.G.,Haworth J.C.,Martin B.,Wood-Steiman P.,Seargeant L.E.,Seifert B.,Booth F.A.,Prasad C.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference31 articles.

1. Glutaric aciduria; a “new” disorder of amino acid metabolism;Goodman;Biochem Med,1975

2. Glutaric aciduria: Inherited deficiency of glutaryl-CoA dehydrogenase activity;Goodman;Biochem Med,1975

3. l-Glutaric acidemia: Investigation of a patient and his family;Whelan;Pediatrics,1979

4. Neurological manifestations of organic acid disorders;Hoffmann;Eur J Pediatr,1994

5. Phenotypic variability in glutaric aciduria type I: Report of fourteen cases in five Canadian Indian kindreds;Haworth;J Pediatr,1991

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