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Published byRatna Irawan Modified over 6 years ago
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CFTR mutation in an Arab patient: Clinical and functional features of 875+1G→A/875+1G→A genotype
Elide Spinelli, Manuela Seia, Paola Melotti, Eleonora Marchina, Rita Padoan Journal of Cystic Fibrosis Volume 8, Issue 4, Pages (July 2009) DOI: /j.jcf Copyright © 2009 European Cystic Fibrosis Society Terms and Conditions
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Fig. 1 The patient's family tree.
Journal of Cystic Fibrosis 2009 8, DOI: ( /j.jcf ) Copyright © 2009 European Cystic Fibrosis Society Terms and Conditions
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Fig. 2 NPD measurements. The agents indicated at the bottom were added at the times (seconds) shown on the x axis. On the y axis, PD are expressed in mV. The graph was obtained during measurements of the left nostril and is representative of both nostrils. Journal of Cystic Fibrosis 2009 8, DOI: ( /j.jcf ) Copyright © 2009 European Cystic Fibrosis Society Terms and Conditions
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