Cargando…
Cost-effective sequence analysis of 113 genes in 1,192 probands with retinitis pigmentosa and Leber congenital amaurosis
Introduction: Retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA) are two groups of inherited retinal diseases (IRDs) where the rod photoreceptors degenerate followed by the cone photoreceptors of the retina. A genetic diagnosis for IRDs is challenging since >280 genes are associated w...
Ejemplares similares
-
Effective smMIPs-Based Sequencing of Maculopathy-Associated Genes in Stargardt Disease Cases and Allied Maculopathies from the UK
por: Mc Clinton, Benjamin, et al.
Publicado: (2023) -
Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease
por: Van de Sompele, Stijn, et al.
Publicado: (2018) -
Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease
por: Van de Sompele, Stijn, et al.
Publicado: (2019) -
Targeted nanopore sequencing enables complete characterisation of structural deletions initially identified using exon‐based short‐read sequencing strategies
por: McClinton, Benjamin, et al.
Publicado: (2023) -
Novel homozygous mutations in the transcription factor NRL cause non-syndromic retinitis pigmentosa
por: El-Asrag, Mohammed E., et al.
Publicado: (2022)