POLG1, C10ORF2, and ANT1 mutations are uncommon in sporadic progressive external ophthalmoplegia with multiple mitochondrial DNA deletions-Reference-Cited by-同舟云学术

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POLG1, C10ORF2, and ANT1 mutations are uncommon in sporadic progressive external ophthalmoplegia with multiple mitochondrial DNA deletions

Published:2006-05-08 Issue:9 Volume:66 Page:1439-1441
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Hudson G.,Deschauer M.,Taylor R. W.,Hanna M. G.,Fialho D.,Schaefer A. M.,He L. -P.,Blakely E.,Turnbull D. M.,Chinnery P. F.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 24 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Expanding the genotype–phenotype correlation of childhood sensory polyneuropathy of genetic origin;Scientific Reports;2020-09-30

2. Clinicogenetical Variants of Progressive External Ophthalmoplegia - An Especial Review of Non-ophthalmic Manifestations;Neurology India;2020

3. Eyelid and Facial Nerve Disorders;Liu, Volpe, and Galetta's Neuro-Ophthalmology;2019

4. Pathogenicity in POLG syndromes: DNA polymerase gamma pathogenicity prediction server and database;BBA Clinical;2017-06

5. Peripheral neuropathy predicts nuclear gene defect in patients with mitochondrial ophthalmoplegia;Brain;2014-10-04

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