लेखक खोज परिणाम

1

Kérwá

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

द्वारा 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

प्रकाशित 2006

संस्थान: Universidad de Costa Rica

Repositorio: Kérwá