Mutations of Wilms' tumor suppressor gene1 (WT1) are associated with embryonic malignancy of the kidney, affecting around 1-9 in 100,000 infants. It occurs in both sporadic and hereditary forms. Inactivation of WT1 causes Wilms tumour, and Denys-Drash syndrome (DDS), leading to nephropathy and genital abnormalities.
Sample Type - Paraffin Block and Slides
Reporting Time - Please Call Customer care
Prerequisites - No special preparation required
Price - ₹5490/-
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