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Това е тежко нелечимо хромозомно заболяване срещащо се с честота 1/3000 - 1/3500 новородени момченца. Генът е разположен в късото рамо на Х-хромозомата и е най--големият ген в човешкия геном. Основният дефект е аномалия на структурния ген, който е отговор...