A novel mutation expands the genetic and clinical spectrum of MYH7-related myopathies

Authors

Nigel F. Clarke, University of Sydney, Sydney, Australia
Kimberly Amburgey, University of Michigan
James Teener, University of Michigan
Sandra Camelo-Piragua, University of Michigan
Akanchha Kesari, Children's National Medical Center, Washington, DC
Jaya Punetha, Children's National Medical Center, Washington, DC
Leigh B. Waddell, University of Sydney, Sydney, Australia
Mark Davis, University of Western Australia
Nigel G. Laing, University of Western Australia
Nicole Monnier, Nationale de la Santé et de la Recherche Médicale, Grenoble, France
Kathryn N. North, University of Sydney, Sydney, Australia
Eric P. Hoffman, George Washington UniversityFollow
James J. Dowling, University of Michigan

Document Type

Journal Article

Publication Date

3-8-2013

Journal

Neuromuscular Disorders

Volume

Volume 23, Issue 5

Inclusive Pages

432-436

Keywords

Cardiac Myosins--genetics; Muscular Diseases--pathology; Mutation--genetics; Myosin Heavy Chains--genetics

APA Citation

Clarke, N. F., Amburgey, K., Teener, J., Camelo-Piragua, S., Kesari, A., Punetha, J., Waddell, L.B., Davis, M., Laing, N.G., Monnier, N., North, K.N., Hoffman, E.P., Dowling, J. J. (2013). A novel mutation expands the genetic and clinical spectrum of MYH7-related myopathies. Neuromuscular Disorders, 23(5), 432-436.

Peer Reviewed

1