Long-term clinical follow-up of a family with Becker muscular dystrophy associated with a large deletion in the DMD gene-Reference-Cited by-同舟云学术

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Long-term clinical follow-up of a family with Becker muscular dystrophy associated with a large deletion in the DMD gene

Published:2024-06 Issue: Volume:39 Page:5-9
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Davies Kay E,Vogt Julie

Funder

Sarepta Therapeutics Inc

Publisher

Elsevier BV

Reference29 articles.

1. Variability and trends in corticosteroid use by male United States participants with Duchenne muscular dystrophy in the Duchenne Registry;Cowen;BMC Neurol,2019

2. Gene therapy for Duchenne muscular dystrophy;Elangkovan;J Neuromuscul Dis,2021

3. Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management;Bushby;Lancet Neurol,2010

4. Systemic AAV Micro-dystrophin Gene Therapy for Duchenne Muscular Dystrophy;Duan;Mol Ther,2018

5. The Dystrophin Complex: Structure, Function, and Implications for Therapy;Gao;Compr Physiol,2015

Cited by 1 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. Corrigendum to “Long-term clinical follow-up of a family with Becker muscular dystrophy associated with a large deletion in the DMD gene” Neuromuscular Disorders 39 (2024) 5–9;Neuromuscular Disorders;2024-06

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