Neurogenetics DNA Diagnostic Laboratory: DNA Mutation Testing for Autosomal Dominant Parkinson Disease (LRRK2, Park8)
- Phone: 617-726-5721
REQUIRED FOR ALL ORDERS
- General Requisition Form
- Test Addition Form
- NCL Checklist
- Sample Preparation
- Consent Form
- Medical Release Form
We offer an expanded targeted sequencing 18/51 exons for DNA mutations in the LRRK2 gene that causes autosomal dominant Parkinson disease.
Sample Preparation: Sample Preparation (PDF)
Results of DNA analysis will be communicated in a written report to the referring professional.
ReasonDNA analysis is appropriate for the study of affected patients, for diagnostic confirmation in a suspected affected patient, and in prenatal testing situations after the family mutation has been identified in the proband.