
StudyFinder
Minnesota Neurogenetics Repository

Status: 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
Sex: Male or Female
Age Group: 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
Conditions:
Rare Diseases, Rare Diseases
Keywords:
Clinics and Surgery Center (CSC), Muscular Dystrophy
Study Contact: Peter Kang - pkang@umn.edu
Principal Investigator: Peter Kang
IRB Number: STUDY00011988