The CRB1 and adherens junction complex proteins in retinal development and maintenance
Author:
Publisher
Elsevier BV
Subject
Sensory Systems,Ophthalmology
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3. Mpdz null allele in an avian model of retinal degeneration and mutations in human Leber congenital amaurosis and retinitis pigmentosa;Ali;Invest. Ophthalmol. Vis. Sci.,2011
4. Microarray and morphological analysis of early postnatal CRB2 mutant retinas on a pure C57BL/6J genetic background;Alves;PLoS One,2013
5. Loss of CRB2 in the mouse retina mimics human retinitis pigmentosa due to mutations in the CRB1 gene;Alves;Hum. Mol. Genet.,2013
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