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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.
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