Genetic heterogeneity in giant axonal neuropathy: an Algerian family not linked to chromosome 16q24.1-Reference-Cited by-同舟云学术

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Genetic heterogeneity in giant axonal neuropathy: an Algerian family not linked to chromosome 16q24.1

Published:2002-11 Issue:9 Volume:12 Page:849-852
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

TAZIR M,VALLAT J,BOMONT P,ZEMMOURI R,SINDOU P,ASSAMI S,NOUIOUA S,HAMMADOUCHE T,GRID D,KOENIG M

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Cited by 27 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. Evaluation of hair structural abnormalities in children with different neurological diseases;The Turkish Journal of Pediatrics;2022

2. Giant axonal neuropathy: a multicenter retrospective study with genotypic spectrum expansion;neurogenetics;2019-10-26

3. Giant axonal neuropathy: Clinical, radiological, and genetic features;Annals of Indian Academy of Neurology;2018

4. Giant axonal disease: Report of eight cases;Brain and Development;2015-09

5. Ataluren treatment of patients with nonsense mutation dystrophinopathy;Muscle & Nerve;2014-09-22

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