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المؤلفون: Emília Vieira, I. Fineza, Márcia E. Oliveira, Teresa Coelho, MJ Fonseca, T. Moreno, Karl Heinimann, Mariana Santos, Samuel I. Pascual-Pascual, Rosário Santos, Paula Jorge, Isabel Soares-Silva, Clara Barbot, Márcia Martins, J Prats, A. Cabral, C. Barbosa, ML Aríztegui, Elsa Bronze-da-Rocha, Jorge Oliveira, J.C. Ferreira, Ana S. P. Moreira
المصدر: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAPمصطلحات موضوعية: Adult, Male, Adolescent, HDE NEU PED, Biology, medicine.disease_cause, Muscular Dystrophies, Loss of heterozygosity, Young Adult, 03 medical and health sciences, Exon, 0302 clinical medicine, Genotype, Genetics, medicine, Humans, Missense mutation, Muscular dystrophy, Child, Gene, Genetics (clinical), 030304 developmental biology, 0303 health sciences, Mutation, Polymorphism, Genetic, Infant, Muscular Dystrophies/congenital, medicine.disease, Laminin/genetics, Child, Preschool, Congenital muscular dystrophy, Female, Laminin, 030217 neurology & neurosurgery, Gene Deletion
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3200a80ea6712a224e0a724d41307916