Human Genetics Laboratory: WFS1 Gene Mutation and Polymorphism Database (RRID:SCR_001113)Copy Citation Copied
URL: http://www.khri.med.umich.edu/research/lesperance_lab/low_freq.php
Proper Citation: Human Genetics Laboratory: WFS1 Gene Mutation and Polymorphism Database (RRID:SCR_001113)
Description: This web site lists the disease causing mutations and polymorphisms found in the Wolfram syndrome (WFS1) gene. Sponsors: This resource is supported by the University of Michigan at Ann Arbor.
Synonyms: WFS1
Resource Type: service resource, storage service resource, data or information resource, data repository, database
Keywords: frequency, gene, auditory, disease, hearing, neuropathy, polymorphism, research, wolfram syndrome
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