A novel variant in IDH3A identified in a case with Leber congenital amaurosis accompanied by macular pseudocoloboma.

A novel variant in IDH3A identified in a case with Leber congenital amaurosis accompanied by macular pseudocoloboma.
Ophthalmic Genet. 2018 Jul 30;:1-2
Authors: Sun W, Zhang Q
PMID: 30058936 [PubMed - as supplied by publisher]

Source: Ophthalmic Genetics - August 1, 2018 Category: Opthalmology Tags: Ophthalmic Genet Source Type: research