CADASIL | Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy

Gene SymbolLocusProtein
NOTCH319p13.2-p13.1Neurogenic locus notch homolog protein 3Locus-SpecificHGMDMore Links

Disease-related information: Reviews cadasil 30877 Resources OMIM
Test Information
Last updated: 05-AUG-2009

Charles University, 1st Faculty of Medicine
Institute of Inherited Metabolic Disorders
Praha, Czech Republic
Methods: Sequence analysis of select exons

Comments: Exons 3-10
Contact: Stan Kmoch, PhD
email: skmoch@lf1.cuni.czphone: +420 2-24967691fax: +420 2-24967168
Laboratory can only accept contact from health care providers. Patients/families are encouraged to discuss genetic testing options with their health care provider.
Clinical Laboratory Information (click here for details)

(Printed: Nov 25 2009 22:33 EST)