SURF1 deficiency causes demyelinating Charcot-Marie-Tooth disease-Reference-Cited by-同舟云学术

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SURF1 deficiency causes demyelinating Charcot-Marie-Tooth disease

Published:2013-09-11 Issue:17 Volume:81 Page:1523-1530
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Echaniz-Laguna A.,Ghezzi D.,Chassagne M.,Mayencon M.,Padet S.,Melchionda L.,Rouvet I.,Lannes B.,Bozon D.,Latour P.,Zeviani M.,Mousson de Camaret B.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 55 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. Biallelic variants inCOX18cause a mitochondrial disorder primarily manifesting as peripheral neuropathy;2024-07-04

2. Alternative splicing expands the clinical spectrum of NDUFS6-related mitochondrial disorders;Genetics in Medicine;2024-06

3. Identification of a Novel Homozygous Mutation in MTMR2 Gene Causes Very Rare Charcot–Marie–Tooth Disease Type 4B1;The Application of Clinical Genetics;2024-05

4. More than Just Bread and Wine: Using Yeast to Understand Inherited Cytochrome Oxidase Deficiencies in Humans;International Journal of Molecular Sciences;2024-03-29

5. Natural History of SURF1 Deficiency: A Retrospective Chart Review;Pediatric Neurology;2023-03

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