Mouse models for muscular dystrophies: an overview-Reference-Cited by-同舟云学术

Mouse models for muscular dystrophies: an overview

Published:2020-02-01 Issue:2 Volume:13 Page:dmm043562
ISSN:1754-8403
Container-title:Disease Models & Mechanisms
language:en
Short-container-title:Dis. Model. Mech.

Author:

van Putten Maaike¹^ORCID,Lloyd Erin M.²,de Greef Jessica C.¹^ORCID,Raz Vered¹^ORCID,Willmann Raffaella³^ORCID,Grounds Miranda D.²^ORCID

Affiliation:

1. Leiden University Medical Center, Department of Human Genetics, Leiden, 2333 ZA, The Netherlands

2. The University of Western Australia, School of Human Sciences, Perth 6009, Australia

3. University of Basel, Biozentrum, Basel, CH-4056, Switzerland

Publisher

The Company of Biologists

Subject

General Biochemistry, Genetics and Molecular Biology,Immunology and Microbiology (miscellaneous),Medicine (miscellaneous),Neuroscience (miscellaneous)

Reference122 articles.

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2. 4th Annual Dysferlin Conference 11–14 September 2010, Washington, USA

3. Animal models for muscular dystrophy: valuable tools for the development of therapies

4. A decline in PABPN1 induces progressive muscle weakness in Oculopharyngeal muscle dystrophy and in muscle aging

5. Targeted Disruption of Exon 52 in the Mouse Dystrophin Gene Induced Muscle Degeneration Similar to That Observed in Duchenne Muscular Dystrophy

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