Bedside diagnosis of rippling muscle disease
- PMID: 21082690
- DOI: 10.1002/mus.21825
Bedside diagnosis of rippling muscle disease
Comment on
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Bedside diagnosis of rippling muscle disease in CAV3 p.A46T mutation carriers.Muscle Nerve. 2010 Jun;41(6):751-7. doi: 10.1002/mus.21589. Muscle Nerve. 2010. PMID: 20229577
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[Rippling muscle disease in children].Zhonghua Er Ke Za Zhi. 2005 Feb;43(2):156-8. Zhonghua Er Ke Za Zhi. 2005. PMID: 15833181 Review. Chinese. No abstract available.
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Rippling muscle disease and facioscapulohumeral dystrophy-like phenotype in a patient carrying a heterozygous CAV3 T78M mutation and a D4Z4 partial deletion: Further evidence for "double trouble" overlapping syndromes.Neuromuscul Disord. 2012 Jun;22(6):534-40. doi: 10.1016/j.nmd.2011.12.001. Epub 2012 Jan 14. Neuromuscul Disord. 2012. PMID: 22245016 Free PMC article.
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