Autosomal dominant neovascular inflammatory vitreoretinopathy with CAPN5 c.731T > C gene mutation; clinical management of a family cohort and review of the literature. - Tabbaa, Tarek; Mehra, Ankur A.; Kesav, Natasha P.; Mahajan, Vinit B.; Swanson, Roy D.; Zubricky, Ryan; Sobol, Warren M. (Ophthalmic Genetics, 2023)