Mutations in phenotypically mildD-2-hydroxyglutaric aciduria-Reference-Cited by-同舟云学术

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Mutations in phenotypically mildD-2-hydroxyglutaric aciduria

Published:2005 Issue:4 Volume:58 Page:626-630
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Struys Eduard A.,Korman Stanley H.,Salomons Gajja S.,Darmin Patricia S.,Achouri Younes,Van Schaftingen Emile,Verhoeven Nanda M.,Jakobs Cornelis

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference8 articles.

1. Mutations in the d-2-Hydroxyglutarate Dehydrogenase Gene Cause d-2-Hydroxyglutaric Aciduria

2. D-2-hydroxyglutaric aciduria: Case report and biochemical studies

3. D-2-Hydroxyglutaric aciduria: Biochemical marker or clinical disease entity?

4. D-2-Hydroxyglutaric aciduria: Further clinical delineation

5. D-2-Hydroxyglutaric Aciduria and Glutaric Aciduria Type 1 in Siblings: Coincidence, or Linked Disorders?

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