Neurologic features and genotype-phenotype correlation in Wolfram syndrome

Identification and Characterization of Wolframin, the Product of the Wolfram Syndrome Gene (WFS1), as a Novel Calmodulin-Binding Protein

(2009) Saki Yurimoto et al.   BIOCHEMISTRY

Mitochondrial abnormalities drive cell death in Wolfram syndrome 2

(2009) Tomotake Kanki et al.   CELL RESEARCH

Cisd2 deficiency drives premature aging and causes mitochondria-mediated defects in mice

(2009) Y.-F. Chen et al.   GENES & DEVELOPMENT

Autosomal dominant transmission of diabetes and congenital hearing impairment secondary to a missense mutation in theWFS1gene

(2008) R. Valro et al.   DIABETIC MEDICINE

Identification of novel mutations of the WFS1 gene in Brazilian patients with Wolfram syndrome

(2008) Maria Regina R Gasparin et al.   EUROPEAN JOURNAL OF ENDOCRINOLOGY

WFS1 mutations are frequent monogenic causes of juvenile-onset diabetes mellitus in Lebanon

(2008) Pierre A. Zalloua et al.   HUMAN MOLECULAR GENETICS