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Kérwá

artículo original

Clinical and molecular diagnosis of a Costa Rican family with autosomal recessive myotonia congenital (Becker disease) carrying a new mutation in the CLCN1 gene

od Morales Montero, Fernando, Cuenca Berger, Patricia, del Valle Carazo, Gerardo, Vásquez Cerdas, Melissa, Brian Gago, Roberto, Sittenfeld Appel, Mauricio, Johnson, Keith, Lin, Xi, Ashizawa, Tetsuo

Izdano 2006

Institucija: Universidad de Costa Rica

Repositorio: Kérwá