Holocarboxylase synthetase deficiency: A biotin-responsive organic acidemia
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference19 articles.
1. β-hydroxyisovaleric aciduria and β-methylcrotonylglycinuria: a new inborn error of metabolism;Eldjarn;Lancet,1970
2. Biotinresponsive β-methylcrotonylglycinuria;Gompertz;Lancet,1971
3. Child with a defect in leucine metabolism associated with β-hydroxyisovaleric aciduria and β-methylcrotonylglycinuria;Gompertz;Arch Dis Child,1973
4. Organic aciduria: Treatable cause of floppy infant syndrome;Keeton;Arch Dis Child,1976
5. Massive excretion of 2-oxoglutaric acid and 3-hydroxyiso-valeric acid in a patient with a deficiency of 3-methylcrotonyl-CoA carboxylase;Finnie;Clin Chim Acta,1976
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