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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: data or information resource, data repository, database, service resource, storage service resource
Keywords: frequency, gene, auditory, disease, hearing, neuropathy, polymorphism, research, wolfram syndrome
Resource Name: Human Genetics Laboratory: WFS1 Gene Mutation and Polymorphism Database
Resource ID: SCR_001113
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Source: SciCrunch Registry (RRID:SCR_005400)
Description: Interactive portal for finding and submitting biomedical resources. Resources within SciCrunch have assigned RRIDs which are used to cite resources in scientific manuscripts. SciCrunch Registry, formerly NIF Registry, provides resources catalog. Allows to add new resources. Allows edit existing resources after registration. Curators are tasked with identifying and registering resources, examining data, writing configuration files to index and display data and keeping contents current.
URL: https://rrid.site/rin/sources/SCR_005400
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