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An AAV-SGCG Dose-Response Study in a γ-Sarcoglycanopathy Mouse Model in the Context of Mechanical Stress

  • Published:2019-06 Issue: Volume:13 Page:494-502
  • ISSN:2329-0501
  • Container-title:Molecular Therapy - Methods & Clinical Development
  • language:en
  • Short-container-title:Molecular Therapy - Methods & Clinical Development

Author:

Israeli David,Cosette Jérémie,Corre Guillaume,Amor Fatima,Poupiot Jérôme,Stockholm Daniel,Montus Marie,Gjata Bernard,Richard Isabelle

Funder

Genopole Research-Evry

University Evry Val d’Essonne

Conseil General de l’Essonne

Region Ile de France

Association Française contre les Myopathies

Publisher

Elsevier BV

Subject

Genetics,Molecular Biology,Molecular Medicine

Reference20 articles.

1. Genotype-phenotype correlations in 35 Brazilian families with sarcoglycanopathies including the description of three novel mutations;Moreira;J. Med. Genet.,2003

2. LGMD 2E in Tunisia is caused by a homozygous missense mutation in beta-sarcoglycan exon 3;Bönnemann;Neuromuscul. Disord.,1998

3. γ-sarcoglycan and dystrophin mutation spectrum in an Algerian cohort;Dalichaouche;Muscle Nerve,2017

4. A founder mutation in the gamma-sarcoglycan gene of gypsies possibly predating their migration out of India;Piccolo;Hum. Mol. Genet.,1996

5. Evidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C);Ben Othmane;Am. J. Hum. Genet.,1995

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