Abstract
Experimental data from some laboratories (increased mitochondrial Ca++ concentration, increased O2 consumption, response to inhibitors, altered enzyme kinetics) point to a deranged mitochondrial function in cystic fibrosis (CF) (Burton and Shapiro, 1989).
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References
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© 1991 Springer Science+Business Media New York
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Picci, L. et al. (1991). 2D-Electrophoresis of Mitochondrial Proteins from Cystic Fibrosis Patients. In: Tsui, LC., Romeo, G., Greger, R., Gorini, S. (eds) The Identification of the CF (Cystic Fibrosis) Gene. Advances in Experimental Medicine and Biology, vol 290. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-5934-0_44
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DOI: https://doi.org/10.1007/978-1-4684-5934-0_44
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