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Year | Number of Results |
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Potential involvement of more than one locus in trait manifestation for individuals with Leber congenital amaurosis.
Hum Genet. 2011 Mar;129(3):319-27. doi: 10.1007/s00439-010-0928-y. Epub 2010 Dec 14.
Hum Genet. 2011.
PMID: 21153841
Free PMC article.
Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel Therapies.
Sheck L, Davies WIL, Moradi P, Robson AG, Kumaran N, Liasis AC, Webster AR, Moore AT, Michaelides M.
Sheck L, et al.
Ophthalmology. 2018 Jun;125(6):894-903. doi: 10.1016/j.ophtha.2017.12.013. Epub 2018 Feb 3.
Ophthalmology. 2018.
PMID: 29398085
Free PMC article.
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Genetic and clinical findings in a Chinese cohort with Leber congenital amaurosis and early onset severe retinal dystrophy.
Xu K, Xie Y, Sun T, Zhang X, Chen C, Li Y.
Xu K, et al.
Br J Ophthalmol. 2020 Jul;104(7):932-937. doi: 10.1136/bjophthalmol-2019-314281. Epub 2019 Oct 19.
Br J Ophthalmol. 2020.
PMID: 31630094
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Clinical and molecular findings in a cohort of 152 Brazilian severe early onset inherited retinal dystrophy patients.
Sallum JMF, Motta FL, Arno G, Porto FBO, Resende RG, Belfort R Jr.
Sallum JMF, et al.
Am J Med Genet C Semin Med Genet. 2020 Sep;184(3):728-752. doi: 10.1002/ajmg.c.31828. Epub 2020 Aug 31.
Am J Med Genet C Semin Med Genet. 2020.
PMID: 32865313
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