A novel homozygous missense mutation in the RPE65 gene in an Iranian family with retinitis pigmentosa

Author:

Nateghi Hadiseh,Parvini Farshid,Fahimi Hossein

Publisher

Elsevier BV

Reference39 articles.

1. A novel de novo nonsense mutation in SALL4 causing duane radial ray syndrome: a case report and expanding the phenotypic spectrum;Ajam-Hosseini;BMC Med. Genet.,2023

2. Comprehensive genotyping reveals RPE65 as the most frequently mutated gene in Leber congenital amaurosis in Denmark;Astuti;Eur. J. Hum. Genet.,2016

3. Homozygous females for a X-linked RPGR-ORF15 mutation in an Iranian family with retinitis pigmentosa;Beigi;Exp. Eye Res.,2021

4. Unravelling the genetic basis of simplex Retinitis pigmentosa cases;Bravo-Gil;Sci. Rep.,2017

5. Diagnostic challenges in retinitis pigmentosa: genotypic multiplicity and phenotypic variability;Chang;Curr. Genomics,2011

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