Multiexon skipping leading to an artificial DMD protein lacking amino acids from exons 45 through 55 could rescue up to 63% of patients with Duchenne muscular dystrophy-Reference-Cited by-同舟云学术

Multiexon skipping leading to an artificial DMD protein lacking amino acids from exons 45 through 55 could rescue up to 63% of patients with Duchenne muscular dystrophy

Published:2007-02 Issue:2 Volume:28 Page:196-202
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Béroud Christophe,Tuffery-Giraud Sylvie,Matsuo Masafumi,Hamroun Dalil,Humbertclaude Véronique,Monnier Nicole,Moizard Marie-Pierre,Voelckel Marie-Antoinette,Calemard Laurence Michel,Boisseau Pierre,Blayau Martine,Philippe Christophe,Cossée Mireille,Pagès Michel,Rivier François,Danos Olivier,Garcia Luis,Claustres Mireille

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference37 articles.

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3. Multiplex Western blotting system for the analysis of muscular dystrophy proteins;Anderson;Am J Pathol,1999

4. Exploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies;Beggs;Am J Hum Genet,1991

5. UMD (Universal Mutation Database): a generic software to build and analyze locus-specific databases;Beroud;Hum Mutat,2000

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