Varaico: Literature-Extracted Genetic Variants

Gene:WFS1
Variant:p.W540*
Back to variants list

WFS1

NM_006005.3:p.W540*

Associated Papers

Search for the most precise diagnosis of monogenic diabetes - the usefulness of short-read NGS method in molecular testing in Polish patients.

Płoszaj T et al.

Acta Diabetologica, 2026

Gonadal function in males with WFS1 spectrum disorder (Wolfram syndrome)-A European cohort perspective.

Rohayem J et al.

Andrology, 2026

Patients with a Wide Range of Disorders Related to WFS1 Gene Variants: Novel Mutations and Genotype-Phenotype Correlations.

Grzybowska-Adamowicz J et al.

Genes, 2024

Genotype and clinical characteristics of patients with Wolfram syndrome and WFS1-related disorders.

Lee EM et al.

Frontiers in Genetics, 2023

37415600 (PubMed )
Supplement: DataSheet1.XLSX › Supplementary_Materials

A phase Ib/IIa clinical trial of dantrolene sodium in patients with Wolfram syndrome.

Abreu D et al.

Jci Insight, 2021

34185708 (PubMed )
Supplement: jciinsight-6-145188-s152.pdf

Fast and Efficient Generation of Isogenic Induced Pluripotent Stem Cell Lines Using Adenine Base Editing.

Nami F et al.

The Crispr Journal, 2021

Clinical and molecular assessment of 13 Iranian families with Wolfram syndrome.

Sobhani M et al.

Endocrine, 2019

Monogenic diabetes syndromes: Locus-specific databases for Alström, Wolfram, and Thiamine-responsive megaloblastic anemia.

Astuti D et al.

Human Mutation, 2017

28432734 (PubMed )
Supplement: HUMU-38-764-s001.xlsx › Sheet1

Dominant ER Stress-Inducing WFS1 Mutations Underlie a Genetic Syndrome of Neonatal/Infancy-Onset Diabetes, Congenital Sensorineural Deafness, and Congenital Cataracts.

De Franco E et al.

Diabetes, 2017

Neuroimaging evidence of deficient axon myelination in Wolfram syndrome.

Lugar HM et al.

Scientific Reports, 2016

26888576 (PubMed )
Supplement: srep21167-s1.pdf

The prevalence of Wolfram syndrome in a paediatric population with diabetes.

Zmysłowska A et al.

Endokrynologia Polska, 2014

Phenotypic characteristics of early Wolfram syndrome.

Marshall BA et al.

Orphanet Journal of Rare Diseases, 2013

Diabetes and neurodegeneration in Wolfram syndrome: a multicenter study of phenotype and genotype.

Rohayem J et al.

Diabetes Care, 2011

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."