Cargando…
RBFOX1 and RBFOX3 Mutations in Rolandic Epilepsy
Partial deletions of the gene encoding the neuronal splicing regulator RBFOX1 have been reported in a range of neurodevelopmental diseases, including idiopathic generalized epilepsy. The RBFOX1 protein and its homologues (RBFOX2 and RBFOX3) regulate alternative splicing of many neuronal transcripts...
Autores principales: | Lal, Dennis, Reinthaler, Eva M., Altmüller, Janine, Toliat, Mohammad R., Thiele, Holger, Nürnberg, Peter, Lerche, Holger, Hahn, Andreas, Møller, Rikke S., Muhle, Hiltrud, Sander, Thomas, Zimprich, Fritz, Neubauer, Bernd A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3765197/ https://www.ncbi.nlm.nih.gov/pubmed/24039908 http://dx.doi.org/10.1371/journal.pone.0073323 |
Ejemplares similares
-
Correction: RBFOX1 and RBFOX3 Mutations in Rolandic Epilepsy
por: Lal, Dennis, et al.
Publicado: (2013) -
Rare gene deletions in genetic generalized and Rolandic epilepsies
por: Jabbari, Kamel, et al.
Publicado: (2018) -
NeuN/Rbfox3 Nuclear and Cytoplasmic Isoforms Differentially Regulate Alternative Splicing and Nonsense-Mediated Decay of Rbfox2
por: Dredge, B. Kate, et al.
Publicado: (2011) -
Increased Probability of Co-Occurrence of Two Rare Diseases in Consanguineous Families and Resolution of a Complex Phenotype by Next Generation Sequencing
por: Lal, Dennis, et al.
Publicado: (2016) -
Upregulation of RBFOX1 in the malformed cortex of patients with intractable epilepsy and in cultured rat neurons
por: WEN, MING, et al.
Publicado: (2015)