Human Genome Epidemiology Literature Finder
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Query Trace: Neuromuscular Diseases and SCN4A[original query] |
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In tandem analysis of CLCN1 and SCN4A greatly enhances mutation detection in families with non-dystrophic myotonia. European journal of human genetics : EJHG 2008 Aug 16 (8): 921-9. Trip Jeroen, Drost Gea, Verbove Dennis J, van der Kooi Anneke J, Kuks Jan B M, Notermans Nicolette C, Verschuuren Jan J, de Visser Marianne, van Engelen Baziel G M, Faber Carin G, Ginjaar Ieke |
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