Autor: Liam Oiknine
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Genotype-based severity scoring system in Wolfram Syndrome: correlation with onset of cardinal symptoms and WFS1 gene variant types
BackgroundWolfram syndrome is a rare genetic disorder characterized by antibody‐negative early‐onset atypical diabetes mellitus, optic nerve atrophy, sensorineural hearing loss, central diabetes insipidus (arginine vasopressin deficiency), and progress…