Identification of the netherton syndrome gens by positional cloning and homozygosity mapping.

Project Information

STEPHANECHAVANAS

Grant agreement ID: QLG1-CT-1999-51238

Project closed

Start date 29 December 1999

End date 28 December 2001

Funded under

• Specific Programme for research, technological development and demonstration on "Quality of life and management of living resources", 1998-2002

Total cost € 114 072,00

EU contribution € 114 072,00

Coordinated by

THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
United Kingdom

Objective

We aim to identify the gene for Netherton syndrome (a life threatening monogenic recessive disease associating ichthyosis, hair dysplasia and atopy) by positional cloning & homozygosity mapping.

Programme(s)

• FP5-LIFE QUALITY - Specific Programme for research, technological development and demonstration on "Quality of life and management of living resources", 1998-2002

Topic(s)

• 1.1.1.-7. - Chronic and degenerative diseases, cancer, diabetes, cardivascular diseases and rare diseases

Call for proposal

Data not available

Funding Scheme

RGI - Research grants (individual fellowships)

Coordinator

THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD

• EU contribution: No data
• Address: Roosevelt Drive ; OX3 7BN OXFORD/HEADINGTON ; United Kingdom
• Total cost: No data