Alternative Splicing at a NAGNAG Acceptor Site as a Novel Phenotype Modifier

Approximately 30% of alleles causing genetic disorders generate premature termination codons (PTCs), which are usually associated with severe phenotypes. However, bypassing the deleterious stop codon can lead to a mild disease outcome. Splicing at NAGNAG tandem splice sites has been reported to resu...

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Detalles Bibliográficos
Autores principales: Hinzpeter, Alexandre, Aissat, Abdel, Sondo, Elvira, Costa, Catherine, Arous, Nicole, Gameiro, Christine, Martin, Natacha, Tarze, Agathe, Weiss, Laurence, de Becdelièvre, Alix, Costes, Bruno, Goossens, Michel, Galietta, Luis J., Girodon, Emmanuelle, Fanen, Pascale
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2951375/
https://www.ncbi.nlm.nih.gov/pubmed/20949073
http://dx.doi.org/10.1371/journal.pgen.1001153

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2951375/
https://www.ncbi.nlm.nih.gov/pubmed/20949073
http://dx.doi.org/10.1371/journal.pgen.1001153

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