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2006 | 1 |
2009 | 1 |
2013 | 1 |
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A G1103R mutation in CRB1 is co-inherited with high hyperopia and Leber congenital amaurosis.
Ophthalmic Genet. 2006 Mar;27(1):15-20. doi: 10.1080/13816810500481840.
Ophthalmic Genet. 2006.
PMID: 16543197
Genetic heterogeneity in two consanguineous families segregating early onset retinal degeneration: the pitfalls of homozygosity mapping.
Benayoun L, Spiegel R, Auslender N, Abbasi AH, Rizel L, Hujeirat Y, Salama I, Garzozi HJ, Allon-Shalev S, Ben-Yosef T.
Benayoun L, et al.
Am J Med Genet A. 2009 Feb 15;149A(4):650-6. doi: 10.1002/ajmg.a.32634.
Am J Med Genet A. 2009.
PMID: 19140180
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Mutations in CRB1 are a relatively common cause of autosomal recessive early-onset retinal degeneration in the Israeli and Palestinian populations.
Beryozkin A, Zelinger L, Bandah-Rozenfeld D, Harel A, Strom TA, Merin S, Chowers I, Banin E, Sharon D.
Beryozkin A, et al.
Invest Ophthalmol Vis Sci. 2013 Mar 1;54(3):2068-75. doi: 10.1167/iovs.12-11419.
Invest Ophthalmol Vis Sci. 2013.
PMID: 23449718
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