Spinal muscular arthrophy gene mutation analysis (exon 7,8)(blood)

Description

A genetic test to detect mutations in the SMN1 gene, specifically exons 7 and 8, associated with spinal muscular atrophy (SMA). Early diagnosis is crucial for managing the disease and considering treatment options, such as gene therapy.

This lab test includes home sample collection via a provided kit or by a clinician, and you'll receive a comprehensive physical health report with your results.