Whole exome sequencing identifies a pathogenic mutation in WFS1 in two large Chinese families with autosomal dominant all-frequency hearing loss and prenatal counseling.
International journal of pediatric otorhinolaryngology 2018 Mar 106 113-119.
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Genotypic classification of patients with Wolfram syndrome: insights into the natural history of the disease and correlation with phenotype.
Genetics in medicine : official journal of the American College of Medical Genetics 2013 Jul 15 (7): 497-506.
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