Novel mutations in LTBP2 identified in familial cases of primary congenital glaucoma.

Conclusions: We identified three novel mutations, p.D1010N, p.Q1143Rfs*35, and p.C1757Y, in LTBP2 responsible for PCG.
PMID: 32165823 [PubMed - in process]

Source: Molecular Vision - March 15, 2020 Category: Molecular Biology Tags: Mol Vis Source Type: research