Moroccan consanguineous family with Becker myotonia and review

por Ratbi, Ilham, Elalaoui, Siham Chafai, Escudero, Adela, Kriouile, Yamina, Molano, Jesus, Sefiani, Abdelaziz
Publicado 2011

Molecular Diagnosis of Limb-girdle Muscular Dystrophy Type 2A by Next-generation Sequencing

por Gómez-González, Clara, Esteban-Rodríguez, Maria Isabel, Ruano, Yolanda, Vallespín, Elena, Lapunzina, Pablo, Martínez, Paloma, Pascual, Samuel I., Molano, Jesús, Prior, Carmen
Publicado 2017

Interplay between DMD Point Mutations and Splicing Signals in Dystrophinopathy Phenotypes

por Juan-Mateu, Jonàs, González-Quereda, Lidia, Rodríguez, Maria José, Verdura, Edgard, Lázaro, Kira, Jou, Cristina, Nascimento, Andrés, Jiménez-Mallebrera, Cecilia, Colomer, Jaume, Monges, Soledad, Lubieniecki, Fabiana, Foncuberta, Maria Eugenia, Pascual-Pascual, Samuel Ignacio, Molano, Jesús, Baiget, Montserrat, Gallano, Pia
Publicado 2013