Mutations of mitochondrial DNA polymerase ?A are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia-Reference-Cited by-同舟云学术

Mutations of mitochondrial DNA polymerase ?A are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia

Published:2002-07-23 Issue:2 Volume:52 Page:211-219
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Lamantea Eleonora,Tiranti Valeria,Bordoni Andreina,Toscano Antonio,Bono Francesco,Servidei Serena,Papadimitriou Alex,Spelbrink Hans,Silvestri Laura,Casari Giorgio,Comi Giacomo P.,Zeviani Massimo

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference36 articles.

1. An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region

2. Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: Clinical, morphologic, and biochemical studies

3. Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia.

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

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