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1.
Whole-exome sequencing reveals ZNF408 as a new gene associated with autosomal recessive retinitis pigmentosa with vitreal alterations.
Hum Mol Genet
; 24(14): 4037-48, 2015 Jul 15.
Article
in English
| MEDLINE | ID: mdl-25882705
2.
Involvement of LCA5 in Leber congenital amaurosis and retinitis pigmentosa in the Spanish population.
Ophthalmology
; 121(1): 399-407, 2014 Jan.
Article
in English
| MEDLINE | ID: mdl-24144451
3.
Exome sequencing extends the phenotypic spectrum for ABHD12 mutations: from syndromic to nonsyndromic retinal degeneration.
Ophthalmology
; 121(8): 1620-7, 2014 Aug.
Article
in English
| MEDLINE | ID: mdl-24697911
4.
Late onset retinitis pigmentosa.
Ophthalmology
; 118(12): 2523-4, 2011 Dec.
Article
in English
| MEDLINE | ID: mdl-22136677
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