Core-rod myopathy caused by mutations in the nebul... [Neurology. 2009] - PubMed

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Lack of the C-terminal domain of nebulin in a patient with nemaline myopathy. [Muscle Nerve. 2002]
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Gurgel-Giannetti J, Bang ML, Reed U, Marie S, Zatz M, Labeit S, Vainzof M. Muscle Nerve. 2002 May; 25(5):747-52.
Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy. [Proc Natl Acad Sci U S A. 1999]
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Pelin K, Hilpelä P, Donner K, Sewry C, Akkari PA, Wilton SD, Wattanasirichaigoon D, Bang ML, Centner T, Hanefeld F, et al. Proc Natl Acad Sci U S A. 1999 Mar 2; 96(5):2305-10.
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Sewry CA, Brown SC, Pelin K, Jungbluth H, Wallgren-Pettersson C, Labeit S, Manzur A, Muntoni F. Neuromuscul Disord. 2001 Mar; 11(2):146-53.
Review Nemaline myopathy: current concepts. The ENMC International Consortium and Nemaline Myopathy. [J Med Genet. 1997]
Review Nemaline myopathy: current concepts. The ENMC International Consortium and Nemaline Myopathy.
North KN, Laing NG, Wallgren-Pettersson C. J Med Genet. 1997 Sep; 34(9):705-13.
Review Nemaline myopathies. [Semin Pediatr Neurol. 2011]
Review Nemaline myopathies.
Wallgren-Pettersson C, Sewry CA, Nowak KJ, Laing NG. Semin Pediatr Neurol. 2011 Dec; 18(4):230-8.

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Cited by 3 PubMed Central articles

Review Nebulin, a major player in muscle health and disease. [FASEB J. 2011]
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Review The Nebulin family: an actin support group. [Trends Cell Biol. 2011]
Review The Nebulin family: an actin support group.
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Core-rod myopathy caused by mutations in the nebulin gene.
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