We have mapped a gene responsible for renal Fanconi syndrome inherited as an autosomal dominant manner. We are currently testing candidate genes in the linkage region for mutations in a proband from the family. It is hoped that identification of the gene will further our knowledge of the pathophysiology of hreditary renal Fanconi syndrome and renal tutublar disorders in general.

Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Intramural Research (Z01)
Project #
1Z01HG000184-01
Application #
6555937
Study Section
(GDRB)
Project Start
Project End
Budget Start
Budget End
Support Year
1
Fiscal Year
2001
Total Cost
Indirect Cost
Name
Human Genome Research
Department
Type
DUNS #
City
State
Country
United States
Zip Code