Genetic Studies of Neurologic and Dementing Disorders
Project Description:
The specific aims of this study are to characterize disease of four specific disease categories and perform linkage analysis; search for causative mutations; and perform genotype/phenotype correlations for two novel neurogenetic diseases recently identified by our group.
The four disease categories to be studied are: (1) hereditary ataxias, (2)non-Alzheimer forms of dementia, (3) two types of neuromuscular diseases and (4) two forms of episodic movement disorders.
This project will increase the understanding of the genetic basis of diseases affecting the cerabral cortex, basal ganglia, cerebellum and peripheral nervous system. The results will also contribute to more accurate meurological diagnosis and genetic counseling of families with these diseases.
Keyword(s):
neurogenetic diseases
Core Function(s):
Performing Research or Evaluation, Developing & Disseminating Information
Area of Emphasis
Health-Related Activities, Quality of Life
Target Audience:
Family Members/Caregivers
Unserved or Under-served Populations:
Specific Groups
Primary Target Audience Geographic Descriptor:
State
COVID-19 Related Data:
N/A