Phenotypic variability in glutaric aciduria type I: Report of fourteen cases in five Canadian Indian kindreds

Author:

Haworth J.C.,Booth F.A.,Chudley A.E.,deGroot G.W.,Dilling L.A.,Goodman S.I.,Greenberg C.R.,Mallory C.J.,McClarty B.M.,Seargeant L.E.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference24 articles.

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

2. Organic acidemias due to defects in lysine oxidation: 2-ketoadipic acidemia and glutaric acidemia;Goodman,1989

3. CT-scan findings in an infant with glutaric aciduria type I;Yager;Dev Med Child Neurol,1988

4. Diagnosis of organic acidemias by gas chromatography-mass spectrometry,1981

5. Interleukin-2-dependent T lymphocytes for the diagnosis and investigation of inherited metabolic disorders;Adolph;Clin Chim Acta,1988

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