Cargando…
Interplay between DMD Point Mutations and Splicing Signals in Dystrophinopathy Phenotypes
DMD nonsense and frameshift mutations lead to severe Duchenne muscular dystrophy while in-frame mutations lead to milder Becker muscular dystrophy. Exceptions are found in 10% of cases and the production of alternatively spliced transcripts is considered a key modifier of disease severity. Several e...
Autores principales: | 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 |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3607557/ https://www.ncbi.nlm.nih.gov/pubmed/23536893 http://dx.doi.org/10.1371/journal.pone.0059916 |
Ejemplares similares
-
DMD Mutations in 576 Dystrophinopathy Families: A Step Forward in Genotype-Phenotype Correlations
por: Juan-Mateu, Jonas, et al.
Publicado: (2015) -
Prognostic value of X-chromosome inactivation in symptomatic female carriers of dystrophinopathy
por: Juan-Mateu, Jonàs, et al.
Publicado: (2012) -
Dystrophinopathy Phenotypes and Modifying Factors in
DMD
Exon 45–55 Deletion
por: Poyatos‐García, Javier, et al.
Publicado: (2022) -
Genotypes and Phenotypes of DMD Small Mutations in Chinese Patients With Dystrophinopathies
por: Wang, Liang, et al.
Publicado: (2019) -
Cardiac care of children with dystrophinopathy and females carrying DMD-gene variations
por: Bourke, John, et al.
Publicado: (2022)