1. Autosomal‐dominant WFS1‐related disorder—Report of a novel WFS1 variant and review of the phenotypic spectrum of autosomal recessive and dominant forms
    Aya Abu‐El‐Haija et al, 2021, American Journal of Medical Genetics Part A CrossRef
  2. Novel Mutations of PAX6 and WFS1 Associated With Congenital Cataract in a Chinese Family
    Dan Sheng et al, 2023, Cureus CrossRef
  3. A novelWFS1variant associated with isolated congenital cataracts
    Angela Krutish et al, 2023, Molecular Case Studies CrossRef