Autor: Hayman, T., Millo, T., Hendler, K., Chowers, I., Gross, M., Banin, E., Sharon, D.
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Whole exome sequencing of 491 individuals with inherited retinal diseases reveals a large spectrum of variants and identification of novel candidate genes
BackgroundInherited retinal diseases (IRDs) include a range of vision loss conditions caused by variants in different genes. The clinical and genetic heterogeneity make identification of the genetic cause challenging. Here, a cohort of 491 unsolved cas…