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BRITISH JOURNAL OF OPHTHALMOLOGY, ISSN 0007-1161, 04/2015, Volume 99, Issue 4, pp. 488 - 492
Background In Arabian children referred with retinal dystrophy, we have observed that a specific biallelic nonsense mutation in the gene encoding tubby-like... 
TUBBY-LIKE PROTEIN-1 | RETINAL DEGENERATION | POPULATION | AMAUROSIS | INVOLVEMENT | DISEASE | GENES | RECESSIVE RETINITIS-PIGMENTOSA | OPHTHALMOLOGY | CHILDREN | FAMILY
Journal Article
Ophthalmology, ISSN 0161-6420, 2013, Volume 120, Issue 6, pp. 1239 - 1246
Journal Article
Journal Article
European Journal of Ophthalmology, ISSN 1120-6721, 07/2012, Volume 22, Issue 4, pp. 647 - 653
PURPOSE. Gene identification in retinitis pigmentosa is a prerequisite to future therapies. Accordingly, autosomal recessive retinitis pigmentosa families were... 
Retinal autofluorescence | Homozygosity mapping | MERTK | Retinitis pigmentosa | PHAGOCYTOSIS | ROD-CONE DYSTROPHY | GENOTYPING MICROARRAY | TUBBY-LIKE PROTEIN-1 | LEBER CONGENITAL AMAUROSIS | RCS RAT | RETINAL DYSTROPHY | GENE | EPITHELIUM | SPLICE-SITE MUTATION | OPHTHALMOLOGY
Journal Article
Journal Article
Journal Article