A novel < em > LTBP2 < /em > gene variant in a Turkish family with juvenile-onset open-angle glaucoma

CONCLUSION: We documented a novel missense mutation in the LTBP2 gene leading to a severe form of JOAG with refractory IOP and progressive optic nerve damage, which seems to show autosomal recessive inheritance.PMID:38557215 | DOI:10.1080/13816810.2024.2331540

Source: Ophthalmic Genetics - April 1, 2024 Category: Opthalmology Authors: Banu Bozkurt Ozkan Ba ğcı Sema Üzüm T ülin Çora Source Type: research