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Resource:Human Genetics Laboratory: WFS1 Gene Mutation and Polymorphism Database

Name: Resource:Human Genetics Laboratory: WFS1 Gene Mutation and Polymorphism Database
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.
Other Name(s): WFS1
Parent Organization: University of Michigan at Ann Arbor; Michigan; USA
Resource Type(s): database, data storage repository
Resource: Resource
URL: http://www.khri.med.umich.edu/research/lesperance_lab/low_freq.php
Id: nif-0000-10276
Keywords: frequency, gene, auditory, disease, hearing, neuropathy, polymorphism, research, wolfram syndrome
Link to OWL / RDF: Download this content as OWL/RDF

Curation status: Curated

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Contributors

Aarnaud, Ccdbuser, Eddy kim, Nifbot2



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Facts about Resource:Human Genetics Laboratory: WFS1 Gene Mutation and Polymorphism DatabaseRDF feed
CurationStatuscurated  +
DefiningCitationhttp://www.khri.med.umich.edu/research/lesperance_lab/low_freq.php  +
Definition

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.
Has default formThis property is a special property in this wiki.Resource  +
Has roleDatabase  +, and Data storage repository  +
Idnif-0000-10276  +
Is part ofUniversity of Michigan at Ann Arbor; Michigan; USA  +
KeywordsFrequency  +, Gene  +, Auditory  +, Disease  +, Hearing  +, Neuropathy  +, Polymorphism  +, Research  +, and Wolfram syndrome  +
LabelResource:Human Genetics Laboratory: WFS1 Gene Mutation and Polymorphism Database  +
ModifiedDate13 October 2010  +
SuperCategoryResource  +
SynonymWFS1  +