The cystic fibrosis transmembrane conductance regulator is a dual ATP and chloride channel.

I.L. Reisin(Harvard University), Horacio F. Cantiello(National University of Santiago del Estero), Richard J. Gregory(Massachusetts General Hospital), Dennis A. Ausiello(Harvard University), Jane F. Amara(Massachusetts General Hospital), Edward Abraham(New York Medical College), A. G. Prat(Harvard University)
Journal of Biological Chemistry
August 1, 1994
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