Autosomal dominant neovascular inflammatory vitreoretinopathy with CAPN5 c.731T > C gene mutation; clinical management of a family cohort and review of the literature.

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Title: Autosomal dominant neovascular inflammatory vitreoretinopathy with CAPN5 c.731T > C gene mutation; clinical management of a family cohort and review of the literature.
Authors: Tabbaa, Tarek1 (AUTHOR), Mehra, Ankur A.1 (AUTHOR), Kesav, Natasha P.1 (AUTHOR), Mahajan, Vinit B.2,3 (AUTHOR), Swanson, Roy D.1 (AUTHOR), Zubricky, Ryan1 (AUTHOR), Sobol, Warren M.1 (AUTHOR) warren.sobol@uhhospitals.org
Source: Ophthalmic Genetics. Dec2023, Vol. 44 Issue 6, p559-567. 9p.
Database: Academic Search Ultimate
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