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Генодиагностика миотонической дистрофии 2 типа (cnbp)
Молекулярно-генетическое исследование, предназначенное для выявления миотонической дистрофии (типа 2). Патологические мутации связаны с увеличением количества тетрануклеотидных повторов CCTG в гене CNBP.