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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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:J Cell Biol
Asıl Yazarlar: Schietroma, Cataldo, Parain, Karine, Estivalet, Amrit, Aghaie, Asadollah, Boutet de Monvel, Jacques, Picaud, Serge, Sahel, José-Alain, Perron, Muriel, El-Amraoui, Aziz, Petit, Christine
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: The Rockefeller University Press 2017
Konular:
Research Articles
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5461027/
https://ncbi.nlm.nih.gov/pubmed/28495838
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1083/jcb.201612030
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