Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Vision and FAM161A[original query] |
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A Nonsense Mutation in FAM161A Is a Recurrent Founder Allele in Dutch and Belgian Individuals With Autosomal Recessive Retinitis Pigmentosa. Investigative ophthalmology & visual science 2015 Nov 56 (12): 7418-26. Van Schil Kristof, Klevering B Jeroen, Leroy Bart P, Pott Jan Willem R, Bandah-Rozenfeld Dikla, Zonneveld-Vrieling Marijke N, Sharon Dror, den Hollander Anneke I, Cremers Frans P M, De Baere Elfride, Collin Rob W J, van den Born L Ingebor |
Identification of the genetic determinants responsible for retinal degeneration in families of Mexican descent. Ophthalmic genetics 2017 Sep 1-7. Villanueva Adda, Biswas Pooja, Kishaba Kameron, Suk John, Tadimeti Keerti, Raghavendra Pongali B, Nadeau Karine, Lamontagne Bruno, Busque Lambert, Geoffroy Steve, Mongrain Ian, Asselin Géraldine, Provost Sylvie, Dubé Marie-Pierre, Nudleman Eric, Ayyagari Rad |
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- Page last updated:Dec 04, 2023
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