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OCR: or gene are a Mutations in the androgen more common cause of male utations are pseudohermaphroditism. Th use several inherited as X-linked defects physiology and syndromes that have similar defect is due to hormone profiles, In some families, the fundan premature the point mutations which le he receptor. termination codons that tru le amino-acid Other point mutations lead t vith hormone substitutions that either inte ly (see Fig. 11.11). binding or DNA binding, sel eceptor gene may In rare instances, deletions in be present. See later: · Complete Testicular Femir or · Incomplete Testicular Fem