Generation of induced pluripotent stem cells (IBMSi027-A) from a patient with hearing loss carrying WFS1 c.2051C > T (p.Ala684Val) variant
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Developmental Biology,General Medicine
Reference3 articles.
1. Autosomal-dominant WFS1-related disorder—Report of a novel WFS1 variant and review of the phenotypic spectrum of autosomal recessive and dominant forms;Abu-El-Haija;Am. J. Med. Genet. A,2021
2. Identification of p. A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment;Rendtorff;Am. J. Med. Genet. A,2011
3. Wolfram syndrome and WFS1 gene;Rigoli;Clin. Genet.,2011
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1. Research progress of autoimmune diseases based on induced pluripotent stem cells;Frontiers in Immunology;2024-04-24
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