Late-onset MNGIE due to partial loss of thymidine phosphorylase activity-Reference-Cited by-同舟云学术

Late-onset MNGIE due to partial loss of thymidine phosphorylase activity

Published:2005 Issue:4 Volume:58 Page:649-652
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Martí Ramon,Verschuuren Jan J. G. M.,Buchman Alan,Hirano Ikuo,Tadesse Saba,van Kuilenburg André B. P.,van Gennip Albert H.,Poorthuis Ben J. H. M.,Hirano Michio

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference13 articles.

1. Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)

2. Thymidine Phosphorylase Gene Mutations in MNGIE, a Human Mitochondrial Disorder

3. Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE): A Disease of Two Genomes

4. Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome

5. Site-specific somatic mitochondrial DNA point mutations in patients with thymidine phosphorylase deficiency

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