StudyFinder
Minnesota Neurogenetics Repository
Recruiting
This research study is for participants who have an inherited neuromuscular disorder or neurogenetic disorder, or family members who are unaffected by such disorders
Male or Female
Not specified
Inclusion Criteria:
-individuals with muscular dystrophy, particularly those without genetic diagnoses and those with indeterminate genetic test findings
• individuals with DNA repair disorders including Cockayne syndrome, trichothiodystrophy, and xeroderma pigmentosum
• family members with a genetic neurological or muscle disease
Exclusion Criteria:
• none
Rare Diseases, Rare Diseases
Clinics and Surgery Center (CSC), Muscular Dystrophy
Peter Kang - pkang@umn.edu
Peter Kang
STUDY00011988