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pro vyhledávání: '"V. V. Shmarin"'
Autor:
V. V. Shmarin, D. A. Pukhalskaya, S. A. Krasovsky, Yu. M. Chudakova, A. V. Martynov, G. V. Shmarina
Publikováno v:
Медицинская иммунология, Vol 26, Iss 5, Pp 1045-1052 (2024)
Cystic fibrosis (CF) is one of the most common autosomal-recessive inherited diseases. The primary genetic defect in CF is aligned CFTR gene mutation which encodes a membrane protein functioning as cAMP-depended chloride channel. Classic phenotypical
Externí odkaz:
https://doaj.org/article/d2bd8462184245d5921303507e9f8409
