Becker muscular dystrophy patients with deletions around exon 51; a promising outlook for exon skipping therapy in Duchenne patients-Reference-Cited by-同舟云学术

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Becker muscular dystrophy patients with deletions around exon 51; a promising outlook for exon skipping therapy in Duchenne patients

Published:2010-04 Issue:4 Volume:20 Page:251-254
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Helderman-van den Enden A.T.J.M.,Straathof C.S.M.,Aartsma-Rus A.,den Dunnen J.T.,Verbist B.M.,Bakker E.,Verschuuren J.J.G.M.,Ginjaar H.B.

Publisher

Elsevier BV

Subject

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

Reference22 articles.

1. Local dystrophin restoration with antisense oligonucleotide PRO051;Van Deutekom;N Engl J Med,2007

2. Theoretic applicability of antisense-mediated exon skipping for Duchenne muscular dystrophy mutations;Aartsma-Rus;Hum Mutat,2009

3. Copy number variation in the genome; the human DMD gene as an example;White;Cytogenet Genome Res,2006

4. Functional ability and muscle force in healthy children and ambulant Duchenne muscular dystrophy patients;Beenakker;Eur J Paediatr Neurol,2005

5. Dystrophin characterization in BMD patients: correlation of abnormal protein with clinical phenotype;Morandi;J Neurol Sci,1995

Cited by 50 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. Further evidence for an attenuated phenotype of in‐frame DMD deletions affecting the central rod domain of dystrophin around exon 48;American Journal of Medical Genetics Part A;2024-08-19

2. DMD deletions underlining mild dystrophinopathies: literature review highlights phenotype-related mutation clusters and provides insights about genetic mechanisms and prognosis;Frontiers in Neurology;2024-01-15

3. Duchenne and Becker muscular dystrophy: Cellular mechanisms, image analysis, and computational models: A review;Cytoskeleton;2024-01-15

4. Systemic deletion of DMD exon 51 rescues clinically severe Duchenne muscular dystrophy in a pig model lacking DMD exon 52;Proceedings of the National Academy of Sciences;2023-07-10

5. Bridging between disorder, prevalence, clinical manifestation and therapeutic management of muscular dystrophy;Research Journal of Pharmacy and Technology;2022-11-24

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