NOVEL intronic CAPN3 Roma mutation alters splicing causing RNA mediated decay

CAPN3 mutations cause a limb girdle muscular dystrophy. Functional characterization of novel mutations facilitates diagnosis of future cases. We have identified a novel (c.1992 + 2T>G) CAPN3 mutation that disrupts the donor splice site of intron 17 splicing out exon 17, with mRNA levels severely...

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Detalles Bibliográficos
Autores principales: Mavillard, Fabiola, Madruga‐Garrido, Marcos, Rivas, Eloy, Servián‐Morilla, Emilia, Ávila‐Polo, Rainiero, Marcos, Irene, Morón, Francisco J., Paradas, Carmen, Cabrera‐Serrano, Macarena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Brief Communications
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856619/
https://www.ncbi.nlm.nih.gov/pubmed/31612648
http://dx.doi.org/10.1002/acn3.50910

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856619/
https://www.ncbi.nlm.nih.gov/pubmed/31612648
http://dx.doi.org/10.1002/acn3.50910

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