Aspects génétiques et moléculaires des dystrophinopathies
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference21 articles.
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3. Dystrophin: More than just the sum of its parts;Le Rumeur;Biochim Biophys Acta,2010
4. Genotype-Phenotype Analysis in 2,405 Patients with a Dystrophinopathy Using the UMD-DMD Database: A Model of Nationwide Knowledgebase;Tuffery-Giraud;Hum Mutat,2009
5. Pseudoexon activation in the DMD gene as a novel mechanism for becker muscular dystrophy;Tuffery-Giraud;Hum Mutat,2003
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1. Diagnosis and management of Becker muscular dystrophy: the French guidelines;Journal of Neurology;2023-07-09
2. Role of Growth Factors and Apoptosis Proteins in Cognitive Disorder Development in Patients with Duchenne Muscular Dystrophy;Muscular Dystrophy - Research Updates and Therapeutic Strategies;2020-12-23
3. Le Western-Blot à la rescousse…;Les Cahiers de Myologie;2017-06
4. Diagnostic des myopathies en Afrique de l’Ouest : expérience de quatre pays;Les Cahiers de Myologie;2017-06
5. Pathogenesis of cognitive disorders in patients with Duchenne muscular dystrophy;Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova;2017
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