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Keratin, type II cytoskeletal 71 (KRT71) is an intermediate filament protein primarily expressed in the inner root sheath of the hair follicle, where it plays a central role in hair formation by contributing to the structural framework that supports hair fiber development and maintenance. Mutations in this gene have been associated with hair disorders such as Hypotrichosis 13 and Familial woolly hair syndrome[1][2][3][4][5][6]. KRT71 belongs to the family of type II keratins, clustered on chromosome 12, and is not classified as a traditional therapeutic target, receptor, or enzyme.
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