Drug-induced readthrough of premature stop codons leads to the stabilization of laminin α2 chain mRNA in CMD myotubes-Reference-Cited by-同舟云学术

Drug-induced readthrough of premature stop codons leads to the stabilization of laminin α2 chain mRNA in CMD myotubes

Published:2008 Issue:2 Volume:10 Page:217-224
ISSN:1099-498X
Container-title:The Journal of Gene Medicine
language:en
Short-container-title:J. Gene Med.

Author:

Allamand Valérie,Bidou Laure,Arakawa Masayuki,Floquet Célia,Shiozuka Masataka,Paturneau-Jouas Marion,Gartioux Corine,Butler-Browne Gillian S.,Mouly Vincent,Rousset Jean-Pierre,Matsuda Ryoichi,Ikeda Daishiro,Guicheney Pascale

Publisher

Wiley

Subject

Genetics (clinical),Drug Discovery,Genetics,Molecular Biology,Molecular Medicine

Reference51 articles.

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3. , . Congenital muscular dystrophies. In Neuromuscular Disorders, Clinical and Molecular Genetics, (ed). John Wiley: Chichester, 1998; 21–57.

4. The Saga of Congenital Muscular Dystrophy

5. Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy

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