Molecular, cellular, and pharmacological therapies for Duchenne/Becker muscular dystrophies-Reference-Cited by-同舟云学术

Molecular, cellular, and pharmacological therapies for Duchenne/Becker muscular dystrophies

Published:2005-06 Issue:8 Volume:19 Page:880-891
ISSN:0892-6638
Container-title:The FASEB Journal
language:en
Short-container-title:FASEB j.

Author:

Chakkalakal Joe V.¹,Thompson Jennifer¹,Parks Robin J.²³,Jasmin Bernard J.¹³

Affiliation:

1. Department of Cellular and Molecular MedicineCentre for Neuromuscular DiseaseFaculty of MedicineUniversity of Ottawa General Campus Ottawa Ontario Canada

2. Department of BiochemistryMicrobiology and ImmunologyFaculty of MedicineUniversity of Ottawa General Campus Ottawa Ontario Canada

3. Ottawa Health Research InstituteMolecular Medicine ProgramOttawa Hospital General Campus Ottawa Ontario Canada

Funder

Canadian Institutes of Health Research

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1096/fj.04-1956rev

Reference146 articles.

1. Population frequencies of inherited neuromuscular diseases—A world survey

2. Neuromuscular disorders in childhood. Old dogmas, new concepts;Dubowitz V.;Arch. Dis. Child.,1975

3. Diagnostic criteria for Duchenne and Becker muscular dystrophy and myotonic dystrophy

4. An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus

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