Adult-onset Wolfram syndrome: a case report of bilateral optic atrophy and compound heterozygous WFS1 gene mutations

Can J Ophthalmol. 2026 Sep 24:S0008-4182(26)00349-2. doi: 10.1016/j.jcjo.2026.08.031. Online ahead of print.

NO ABSTRACT

PMID:42785371 | DOI:10.1016/j.jcjo.2026.08.031