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Autor:
J. S. Kaczmarek, M. Maderia, Ronald K. Scheule, Ingrid Mechin, S. Bercury, G. D. Hurlbut, R. Ziegler, A. Nair, J. Bajko, A. Majewski, K. S. Simon, Joseph D. Batchelor, B. J. Hilbert, P. Manavalan, K. Nagarajan, C. Duffy, S. Altmann, M. Kothe, J. Foley
Cystic fibrosis (CF) results from mutations within the gene encoding the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR), a transmembrane chloride channel found on the apical surface of epithelial cells. The most common CF-causing mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::429cdfcd0325476fa4bb776f012e3d72
