Biopolym. Cell. 1990; 6(2):12-17.
Стан і перспективи генної терапії спадкового дефіциту α1-інгібітора протеаз
1Бужиєвська Т. И., 1Черненко В. Ю., 1Поліщук Л. А.
  1. Інститут молекулярної біології і генетики АН УСРС
    Київ, СРСР

Abstract

Викладено молекулярно-генетичні основи спадкового дефіциту α-інгібіторів протеаз, наведено огляд літературних даних існуючих сучасних підходів до генної терапії даної патології у людини.

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