Homozygosity Mapping Reveals Null Mutations in <em>FAM161A</em> as a Cause of Autosomal-Recessive Retinitis Pigmentosa期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

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*Homozygosity Mapping Reveals Null Mutations in FAM161A* as a Cause of Autosomal-Recessive Retinitis Pigmentosa**

Authors:	Dikla Bandah-Rozenfeld Chen Farhy Itay Chowers Saul Merin Ruth Ashery-Padan Dror Sharon

Institution:	¹ Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem 91120, Israel ² Human Molecular Genetics and Biochemistry, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv 69978, Israel ³ The St. John Eye Hospital, Jerusalem 97200, Israel ⁴ Genetics Department, Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa 31096, Israel

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