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Research Models and Gene Augmentation Therapy for CRB1 Retinal Dystrophies
Discuss the recent advances, advantages and disadvantages of different CRB1 human and animal retinal degeneration models.
Aug 14, 2020


Investigating the CRB1 gene and immune system in patients with retinal dystrophy
Retinal death can be caused by several genes. When there is an error in the CRB1 gene, some people become severely visually impaired.
Jul 29, 2020


Clinical and genetic characteristics of 251 consecutive patients with macular and cone/cone-rod dystrophy
Johannes Birtel , Tobias Eisenberger , Martin Gliem , Philipp L. Müller , Philipp Herrmann , Christian Betz , Diana Zahnleiter ,...
Mar 19, 2018

A clinical and molecular characterisation of CRB1-associated maculopathy
These findings show that the rare CRB1 variant, c.498_506del, is strongly associated with localised retinal dysfunction.
Feb 1, 2018

Mutations in CRB1
Data show that CRB1 mutations are a relatively frequent cause of early-onset retinal degeneration in the Israeli and Palestinian population.
Mar 15, 2013

CRB1 mutations in inherited retinal dystrophies
CLRN1, is a four-transmembrane protein predicted to be associated with ribbon synapses of photoreceptors and cochlear hair cells,
Dec 27, 2011
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