USH2A variants causing retinitis pigmentosa or Usher syndrome provoke differential retinal phenotypes in disease-specific organoids-Reference-Cited by-同舟云学术

USH2A variants causing retinitis pigmentosa or Usher syndrome provoke differential retinal phenotypes in disease-specific organoids

Published:2023-10 Issue:4 Volume:4 Page:100229
ISSN:2666-2477
Container-title:Human Genetics and Genomics Advances
language:en
Short-container-title:Human Genetics and Genomics Advances

Author:

Sanjurjo-Soriano Carla,Jimenez-Medina Carla,Erkilic Nejla,Cappellino Luisina,Lefevre Arnaud,Nagel-Wolfrum Kerstin,Wolfrum Uwe,Van Wijk Erwin,Roux Anne-Françoise,Meunier Isabelle,Kalatzis Vasiliki^ORCID

Funder

Gelderse Blinden Stichting

UNADEV

Deutsche Forschungsgemeinschaft

ANR

Fondation de France

Publisher

Elsevier BV

Subject

Genetics (clinical),Molecular Medicine

Reference65 articles.

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2. Photoreceptor degeneration: genetic and mechanistic dissection of a complex trait;Wright;Nat. Rev. Genet.,2010

3. Non-syndromic retinitis pigmentosa;Verbakel;Prog. Retin. Eye Res.,2018

4. Retinitis pigmentosa;Hamel;Orphanet J. Rare Dis.,2006

5. Frequency of Usher syndrome in two pediatric populations: implications for genetic screening of deaf and hard of hearing children;Kimberling;Genet. Med.,2010

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