In tandem analysis of CLCN1 and SCN4A greatly enhances mutation detection in families with non-dystrophic myotonia von 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 B

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Sarcoglycanopathies and the risk of undetected deletion alleles in diagnosis von White, Stefan J., de Willige, Shirley Uitte, Verbove, Dennis, Politano, Luisa, Ginjaar, Ieke, Breuning, Martijn H., den Dunnen, Johan T.

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