Usher syndrome type 1–associated cadherins shape the photoreceptor outer segment

Usher syndrome type 1 (USH1) causes combined hearing and sight defects, but how mutations in USH1 genes lead to retinal dystrophy in patients remains elusive. The USH1 protein complex is associated with calyceal processes, which are microvilli of unknown function surrounding the base of the photorec...

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Detalles Bibliográficos
Autores principales: Schietroma, Cataldo, Parain, Karine, Estivalet, Amrit, Aghaie, Asadollah, Boutet de Monvel, Jacques, Picaud, Serge, Sahel, José-Alain, Perron, Muriel, El-Amraoui, Aziz, Petit, Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2017
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461027/
https://www.ncbi.nlm.nih.gov/pubmed/28495838
http://dx.doi.org/10.1083/jcb.201612030

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461027/
https://www.ncbi.nlm.nih.gov/pubmed/28495838
http://dx.doi.org/10.1083/jcb.201612030

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