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In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathy.

Lookup NU author(s): Professor Patrick Chinnery, Professor Volker StraubORCiD, Emerita Professor Katherine Bushby

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Author(s): Shatunov A, Olivé M, Odgerel Z, Stadelmann-Nessler C, Irlbacher K, Landeghem vanF, Bayarsaikhan M, Lee HS, Goudeau B, Chinnery PF, Straub V, Hilton-Jones D, Damian MS, Kaminska A, Vicart P, Bushby K, Dalakas MC, Sambuughin N, Ferrer I, Goebel HH, Goldfarb LG

Publication type: Article

Publication status: Published

Journal: European Journal of Human Genetics

Year: 2009

Volume: 17

Issue: 5

Pages: 656-63

ISSN (print): 1018-4813

ISSN (electronic): 1476-5438

Publisher: European Journal of Human Genetics

URL: http://dx.doi.org/10.1038/ejhg.2008.226

DOI: 10.1038/ejhg.2008.226


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Funding

Funder referenceFunder name
UK National Commissioning Group
Centro de Investigacion Biomedica en Red de Enfermedades Neurodegenerativas (CIBERNED), Spain
National Institute of Neurological Disorders and Stroke
National Institutes of Health
036825TREAT-NMD EU Network of Excellence
06-MRAR-039-01ANR
12986AFM
FIS 05-1213

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