The first genetic landscape of inherited retinal dystrophies in Portuguese patients identifies recurrent homozygous mutations as a frequent cause of pathogenesis

Inherited retinal diseases (IRDs) are a group of ocular conditions characterized by an elevated genetic and clinical heterogeneity. They are transmitted almost invariantly as monogenic traits. However, with more than 280 disease genes identified so far, association of clinical phenotypes with genoty...

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Detalles Bibliográficos
Autores principales: Peter, Virginie G, Kaminska, Karolina, Santos, Cristina, Quinodoz, Mathieu, Cancellieri, Francesca, Cisarova, Katarina, Pescini Gobert, Rosanna, Rodrigues, Raquel, Custódio, Sónia, Paris, Liliana P, Sousa, Ana Berta, Coutinho Santos, Luisa, Rivolta, Carlo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Biological, Health, and Medical Sciences
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10003751/
https://www.ncbi.nlm.nih.gov/pubmed/36909829
http://dx.doi.org/10.1093/pnasnexus/pgad043

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10003751/
https://www.ncbi.nlm.nih.gov/pubmed/36909829
http://dx.doi.org/10.1093/pnasnexus/pgad043

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