Synonymous Variant in the CHM Gene Causes Aberrant Splicing in Choroideremia

PURPOSE: Choroideremia is an inherited retinal degeneration caused by 280 different pathogenic variants in the CHM gene. Only one silent/synonymous variant (c.1359C>T; p.(Ser453=)) has been reported and was classified as inconclusive based on in silico analysis. This study elucidates the pathogen...

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Detalles Bibliográficos
Autores principales: da Palma, Mariana Matioli, Motta, Fabiana Louise, Gomes, Caio Perez, Salles, Mariana Vallim, Pesquero, João Bosco, Sallum, Juliana Maria Ferraz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2020
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7329626/
https://www.ncbi.nlm.nih.gov/pubmed/32097478
http://dx.doi.org/10.1167/iovs.61.2.38

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7329626/
https://www.ncbi.nlm.nih.gov/pubmed/32097478
http://dx.doi.org/10.1167/iovs.61.2.38

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