Clinical and molecular heterogeneity in very–long-chain acyl-coenzyme a dehydrogenase deficiency-Reference-Cited by-同舟云学术

Clinical and molecular heterogeneity in very–long-chain acyl-coenzyme a dehydrogenase deficiency

Published:2000-02 Issue:2 Volume:22 Page:98-105
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Pons Roser,Cavadini Patrizia,Baratta Silvia,Invernizzi Federica,Lamantea Eleonora,Garavaglia Barbara,Taroni Franco

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health

Reference43 articles.

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4. Hale DE, Stanley CA, Coates PM. The long-chain acyl-CoA dehydrogenase deficiency. In: Tanaka K, Coates PM, eds. Fatty acid oxidation: Clinical, biochemical, and molecular aspects. New York: Alan R. Liss, 1990:303–11.

5. Disorders of mitochondrial long-chain fatty acid oxidation;Pollitt;J Inherit Metab Dis,1995

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