In congenital dystrophic variety of epidermolysis bullosa, mutation is seen in the gene conding for
High-Yield Explanation
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