Neurofibromatosis, type I (NF1), is inherited as a dominant trait, and is extremely common, affecting approximately one in every 3,500 individuals worldwide. The disorder is highly variable in its clinical presentation, and only one-third of affected individuals develop medical complications severe enough to require intervention. It is not known if specific mutations of the NF1 gene are associated with specific clinical presentations. The objective of this protocol is to determine if patients with similar clinical syndromes have similar NF1 mutations. Because some NF1 patients develop malignant changes in their previously benign neurofibromas, Dr. Viskochil is attempting to identify additional mutations as tumors progress from benign to malignant. These studies are being done in cooperation with Dr. Jan Friedman at the University of British Columbia.

Project Start
1999-12-01
Project End
2001-02-28
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
36
Fiscal Year
2000
Total Cost
$1,624
Indirect Cost
Name
University of Utah
Department
Type
DUNS #
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
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