Screening for mutations in Spanish families with myotonia. Functional analysis of novel mutations in CLCN1 gene

dc.contributor.author	Mazón Calpena, María Jesús
dc.contributor.author	Barros de la Roza, Francisco
dc.contributor.author	Peña Cortines, María del Pilar de la
dc.date.accessioned	2013-01-30T10:04:23Z
dc.date.available	2013-01-30T10:04:23Z
dc.date.issued	2012
dc.identifier.citation	Neuromuscular Disorders, 22(3), P. 231–243, (2012); doi:10.1016/j.nmd.2011.10.013	spa
dc.identifier.issn	0960-8966
dc.identifier.uri	http://hdl.handle.net/10651/7717
dc.description.statementofresponsibility	Mazón, M.J., Barros, F., De la Peña, P., Quesada, J.F., Escudero, A., Cobo, A.M., Pascual-Pascual, S.I., Gutiérrez-Rivas, E., Guillén, E., Arpa, J., Eraso, P., Portillo, F., Molano, J.
dc.language.iso	eng
dc.relation.ispartof	Neuromuscular Disorders	eng
dc.source	SCOPUS	spa
dc.title	Screening for mutations in Spanish families with myotonia. Functional analysis of novel mutations in CLCN1 gene	eng
dc.type	journal article
dc.identifier.local	20111645	spa
dc.identifier.doi	10.1016/j.nmd.2011.10.013
dc.relation.publisherversion	http://dx.doi.org/10.1016/j.nmd.2011.10.013	spa

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