Wolfram syndrome in the Japanese population; molecular analysis of WFS1 gene and characterization of clinical features.

<h4>Background</h4>Wolfram syndrome (WFS) is a recessive neurologic and endocrinologic degenerative disorder, and is also known as DIDMOAD (Diabetes Insipidus, early-onset Diabetes Mellitus, progressive Optic Atrophy and Deafness) syndrome. Most affected individuals carry recessive mutations in the ... View More