A 5-year-old Caucasian male is brought to your genetics clinic. His past medical history is significant for diffuse erythema, scaling, and freckle-like areas of increased pigmentation over areas of his body after sunlight exposure. You diagnose him with xeroderma pigmentosum and explain to the mother that it is a hereditary condition resulting in uncorrected DNA mutations that may lead to skin cancer due to what type of defective gene?
A. Apoptotic gene
B. Proto-oncogene
C. Tumor suppressor
D. DNA repair gene
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