A novel D104G mutation in the adenine nucleotide translocator 1 gene in autosomal dominant progressive external ophthalmoplegia patients with mitochondrial DNA with multiple deletions-Reference-Cited by-同舟云学术

A novel D104G mutation in the adenine nucleotide translocator 1 gene in autosomal dominant progressive external ophthalmoplegia patients with mitochondrial DNA with multiple deletions

Published:2002-04-30 Issue:5 Volume:51 Page:645-648
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Komaki Hirofumi,Fukazawa Toshiyuki,Houzen Hideki,Yoshida Kazuto,Nonaka Ikuya,Goto Yu-Ichi

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference18 articles.

1. Mitochondrial DNA and disease

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

3. Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: Clinical, biochemical, and molecular genetic features of the 1Oq-linked disease

4. A Third Locus Predisposing to Multiple Deletions of mtDNA in Autosomal Dominant Progressive External Ophthalmoplegia

5. Role of Adenine Nucleotide Translocator 1 in mtDNA Maintenance

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