Painel Genético para Síndrome de Gorlin-Goltz (NGS) | Sequenciamento dos genes SUFU e PTCH1
This genetic test investigates mutations associated with Gorlin-Goltz syndrome, which is linked to multiple basal cell carcinomas and other systemic changes. It analyzes PTCH1, PTCH2, and SUFU genes.
- The description claims the syndrome is associated with early and multiple basal cell carcinomas.
Variants (1)
- Default Title — 2250.00 BRL — Out of stock
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