Pyruvate dehydrogenase deficiency: Clinical and biochemical diagnosis-Reference-Cited by-同舟云学术

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Pyruvate dehydrogenase deficiency: Clinical and biochemical diagnosis

Published:1993-05 Issue:3 Volume:9 Page:216-220
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

De Meirleir Linda,Lissens Willy,Denis Robert,Wayenberg Jean-Louis,Michotte Alex,Brucher Jean-Marie,Vamos Esther,Gerlo Erik,Liebaers Inge

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,Neurology,Pediatrics, Perinatology and Child Health

Reference21 articles.

1. The genetic heterogeneity of lactic acidosis: Occurrence of recognizable inborn errors of metabolism in a pediatric population with lactic acidosis;Robinson;Pediatr Res,1981

2. The human pyruvate dehydrogenase complex;Dahl;J Biol Chem,1987

3. Isolation of a full-length complementary DNA coding for human E1-α subunit of the pyruvate dehydrogenase complex;De Meirleir;J Biol Chem,1988

4. Cloning and sequencing of cDNA encoding α and β subunits of human pyruvate dehydrogenase;Koike,1988

5. Characterization of cDNA's encoding human pyruvate dehydrogenase α subunit;Ho,1989

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