Natural history of 15 patients with autosomal dominant WFS1 pathogenic variants associated with sensorineural hearing loss and optic atrophy

Wolfram syndrome

Orphanet J Rare Dis. 2026 Apr 18. doi: 10.1186/s13023-026-04348-9. Online ahead of print.

NO ABSTRACT

PMID:42001184 | DOI:10.1186/s13023-026-04348-9