Mutations in GDAP1: Autosomal recessive CMT with demyelination and axonopathy-Reference-Cited by-同舟云学术

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Mutations in GDAP1: Autosomal recessive CMT with demyelination and axonopathy

Published:2002-12-24 Issue:12 Volume:59 Page:1865-1872
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Nelis E.,Erdem S.,Van den Bergh P. Y.K.,Belpaire-Dethiou M.-C.,Ceuterick C.,Van Gerwen V.,Cuesta A.,Pedrola L.,Palau F.,Gabreels-Festen A. A.W.M.,Verellen C.,Tan E.,Demirci M.,Van Broeckhoven C.,De Jonghe P.,Topaloglu H.,Timmerman V.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 148 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. Mutational screening of GDAP1 in dysphonia associated with Charcot-Marie-Tooth disease: clinical insights and phenotypic effects;Journal of Genetic Engineering and Biotechnology;2023-12

2. Homozygous Mutations in GDAP1 and MFN2 Genes Resulted in Autosomal Recessive Forms of Charcot–Marie–Tooth Disease in Consanguineous Pakistani Families;DNA and Cell Biology;2023-11-01

3. Rapid degeneration of iPSC-derived motor neurons lacking Gdap1 engages a mitochondrial-sustained innate immune response;Cell Death Discovery;2023-07-01

4. Conserved intramolecular networks in GDAP1 are closely connected to CMT-linked mutations and protein stability;PLOS ONE;2023-04-14

5. GDAP1 binds 4-hydroxynonenal, the toxic end-product of lipid peroxidation, using its GST-like binding pocket;2022-10-28

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