Analysis of ATP7B in Screening for Wilson Disease

Award Information
Agency:
Department of Health and Human Services
Amount:
$99,444.00
Program:
SBIR
Contract:
1R43DK067764-01
Solitcitation Year:
2004
Solicitation Number:
PHS2004-2
Branch:
N/A
Award Year:
2004
Phase:
Phase I
Agency Tracking Number:
DK067764
Solicitation Topic Code:
N/A
Small Business Information
IDAHO TECHNOLOGY
390 WAKARA WAY, SALT LAKE CITY, UT, 84108
Hubzone Owned:
N
Woman Owned:
N
Socially and Economically Disadvantaged:
N
Duns:
N/A
Principal Investigator
 STEVEN Dobrowolski
 (801) 736-6354
 STEVEN_DOBROWOLSKI@IDAHOTECH.COM
Business Contact
Phone: (801) 582-5138
Research Institution
N/A
Abstract
DESCRIPTION (provided by applicant): Wilson Disease (WD) is an autosomal recessive disorder of copper metabolism. Prospective screening for WD has been proposed however a sensitive and specific biochemical genetic assay was not available and primary molec

* information listed above is at the time of submission.

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