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29. [Different manifestations of tapetoretinal degeneration in the same family (author's transl)]. Fiore C J Fr Ophtalmol; 1981; 4(5):431-40. PubMed ID: 7310068 [TBL] [Abstract][Full Text] [Related]
30. A common founder mutation of CERKL underlies autosomal recessive retinal degeneration with early macular involvement among Yemenite Jews. Auslender N; Sharon D; Abbasi AH; Garzozi HJ; Banin E; Ben-Yosef T Invest Ophthalmol Vis Sci; 2007 Dec; 48(12):5431-8. PubMed ID: 18055789 [TBL] [Abstract][Full Text] [Related]
31. The syndrome of retinal pigmentary degeneration, microcephaly, and severe mental retardation (Mirhosseini-Holmes-Walton syndrome): report of two patients. Mendez HM; Paskulin GA; Vallandro C Am J Med Genet; 1985 Oct; 22(2):223-8. PubMed ID: 4050854 [TBL] [Abstract][Full Text] [Related]