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Human Genetics Laboratory: WFS1 Gene Mutation and Polymorphism Database

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.

URL: http://www.khri.med.umich.edu/research/lesperance_lab/low_freq.php

Resource ID: nif-0000-10276     Resource Type: Resource     Version: Latest Version

Keywords

frequency, gene, auditory, disease, hearing, neuropathy, polymorphism, research, wolfram syndrome

Synonyms

WFS1

Curation Status

uncurated

Additional Resource Types

data repository, database

Supercategory

Resource

Resource Status

Last checked up;

Parent Organization

Original Submitter

Anonymous

Version Status

Curated

Submitted On

12:00am September 21, 2010

Originated From

SciCrunch

Changes from Previous Version

First Version

Version 1

Created 4 years ago by Anonymous