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A mutation in myotilin causes spheroid body myopathy

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Year: 2005
Type: article
Study design: Observational Study
Source: Neurology
DOI: 10.1212/01.wnl.0000188872.28149.9a
Authors: T. Foroud, N. Pankratz, A. P. Batchman, M. W. Pauciulo, R. Vidal, L. Miravalle, H. H. Goebel, L. J. Cushman, B. Azzarelli, H. Horak, M. Farlow, W. C. Nichols
Institutions: Cincinnati Children's Hospital Medical Center, Indiana University Indianapolis, Indiana University School of Medicine, Indiana University – Purdue University Indianapolis
Language: English

Topic: Muscle Physiology and Disorders
Subfield: Molecular Biology
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed

Funders: Purdue University, National Center for Research Resources
Awards: G14405488, General Clinical Research Center
OpenAlex ID: W2115437671
FWCI: 2.133
Cites: 15
Cited by: 88
Related to: 10
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