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Investigative ophthalmology & visual science, ISSN 0146-0404, 11/2015, Volume 56, Issue 12, pp. 7418 - 7426
PURPOSE. To identify mutations in FAM161A underlying autosomal recessive retinitis pigmentosa (arRP) in the Dutch and Belgian populations and to investigate... 
Journal Article
Human Gene Therapy, ISSN 1043-0342, 12/2010, Volume 21, Issue 12, pp. 1749 - 1757
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2010, Volume 87, Issue 2, pp. 199 - 208
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 09/2010, Volume 87, Issue 3, p. 382
Retinitis pigmentosa (RP) is a heterogeneous group of inherited retinal degenerations caused by mutations in at least 45 genes. Using homozygosity mapping, we... 
Proteins | Embryology | Rodents | Retina | Mutation | Gene expression | Chromosomes
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 02/2011, Volume 88, Issue 2, p. 207
Retinitis pigmentosa (RP) is a heterogeneous group of inherited retinal degenerations caused by mutations in at least 50 genes. Using homozygosity mapping in... 
Enzymes | Tissue | Jews | Retina | Glycosylation | Mutation | Gene expression | Patients
Journal Article
Investigative Opthalmology & Visual Science, ISSN 1552-5783, 03/2013, Volume 54, Issue 3, p. 2068
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 08/2010, Volume 87, Issue 2, p. 199
Retinitis pigmentosa (RP) is a heterogeneous group of inherited retinal diseases caused by progressive degeneration of the photoreceptor cells. Using... 
Genes | Arabs | Retina | Eye diseases | Genetics | Mutation | Chromosomes
Journal Article
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