In congenital dystrophic variety of epidermolysis bullosa, mutation is seen in the gene conding for
Correct Answer: Co11agen type 7
Description: Dystrophic epidermolysis bullosa - collagen type VII Epidermolysis bullosa simplex -keratin 14 Junctional epidermolysis bullosa is an inherited disease affecting laminin and collagen . page no. 287. Reference IADVL's concise textbook of dermatology
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