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WFS1 gene

Discuss publications and research concerning the WFS1 gene.

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Related literature

Revision of diagnosis in a child with type 1 diabetes mellitus due to appropriate genetic testing - Wolfram Syndrome.
WFS1
New insights into the complex genetic architecture of age-related hearing loss.
WFS1
Integrative genetic and functional analysis of autosomal dominant hearing loss in 108 multigenerational families.
WFS1
Topology of WFS1 Variants Linked With Islet Function and Higher Risk of Urological Symptoms in WFS1-Associated Disease.
WFS1
A novel mutation of WFS1 gene in a Chinese patient with Wolfram syndrome: a case report.
WFS1
The Application of Next-Generation Sequencing for Mutation Detection in Autosomal-Dominant Hereditary Hearing Impairment.
WFS1
A p.(Glu809Lys) Mutation in the WFS1 Gene Associated with Wolfram-like Syndrome: A Case Report.
WFS1
Bipolar Disorder Type 1 in a 17-Year-Old Girl with Wolfram Syndrome.
WFS1
Expression pattern of wolframin, the WFS1 (Wolfram syndrome-1 gene) product, in common marmoset (Callithrix jacchus) cochlea.
WFS1
Identification of unsuspected Wolfram syndrome cases through clinical assessment and WFS1 gene screening in type 1 diabetes mellitus patients.
WFS1

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