Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Anatomy Item Literature (1447) Expression Attributions Wiki
XB-ANAT-10

Papers associated with retina (and mcc)

Limit to papers also referencing gene:
Show all retina papers
???pagination.result.count???

???pagination.result.page??? 1

Sort Newest To Oldest Sort Oldest To Newest

DLG5 variants are associated with multiple congenital anomalies including ciliopathy phenotypes., Marquez J., J Med Genet. July 1, 2021; 58 (7): 453-464.                        

Nucleoporin NUP205 plays a critical role in cilia and congenital disease., Marquez J., Dev Biol. January 1, 2021; 469 46-53.                        

The Frog Xenopus as a Model to Study Joubert Syndrome: The Case of a Human Patient With Compound Heterozygous Variants in PIBF1., Ott T., Front Physiol. January 1, 2019; 10 134.                

Radial intercalation is regulated by the Par complex and the microtubule-stabilizing protein CLAMP/Spef1., Werner ME., J Cell Biol. August 4, 2014; 206 (3): 367-76.          

???pagination.result.page??? 1