Postoperative Macular Proliferative Vitreoretinopathy: A Case Series and Literature Review

by Samer Khateb, Hamzah Aweidah, Michael Halpert, Tareq Jaouni
Published 2021-05-01

Exome sequencing identifies a founder frameshift mutation in an alternative exon of USH1C as the cause of autosomal recessive retinitis pigmentosa with late-onset hearing loss.

by Samer Khateb, Lina Zelinger, Tamar Ben-Yosef, Saul Merin, Ornit Crystal-Shalit, Menachem Gross, Eyal Banin, Dror Sharon
Published 2012-01-01