Результаты поиска авторов

1

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

по 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

Опубликовано 2006

Институт: Universidad de Costa Rica

Repositorio: Kérwá

2

Kérwá

artículo original

Somatic instability of the expanded CTG triplet repeat in myotonic dystrophy type 1 is a heritable quantitative trait and modifier of disease severity

по Higham, Catherine, Hogg, Grant, Braida, Claudia, del Valle Carazo, Gerardo, Brian Gago, Roberto, Sittenfeld Appel, Mauricio, Ashizawa, Tetsuo, Wilcox, Alison, Couto, Jillian M., Morales Montero, Fernando, Cuenca Berger, Patricia, Wilson, Richard H., Adam, Berit, Wilcox, Dougals E., Monckton, Darren G.

Опубликовано 2012

Институт: Universidad de Costa Rica

Repositorio: Kérwá