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In tandem analysis of CLCN1 and SCN4A greatly enhances mutation detection in families with non-dystrophic myotonia
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 GVolume:
16
Year:
2008
Language:
english
Pages:
9
DOI:
10.1038/ejhg.2008.39
File:
PDF, 191 KB
english, 2008