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Preclinical Studies of a Rare CF-Causing Mutation in the Se..:
Laselva, Onofrio
;
McCormack, Jacqueline
;
Bartlett, Claire
...
Journal of Personalized Medicine. 10 (2020) 4 - p. 209 , 2020
Link:
https://doi.org/10.3390/jpm10040209
RT Journal T1
Preclinical Studies of a Rare CF-Causing Mutation in the Second Nucleotide Binding Domain (c.3700A>G) Show Robust Functional Rescue in Primary Nasal Cultures by Novel CFTR Modulators
UL https://suche.suub.uni-bremen.de/peid=cr-10.3390_jpm10040209&Exemplar=1&LAN=DE A1 Laselva, Onofrio A1 McCormack, Jacqueline A1 Bartlett, Claire A1 Ip, Wan A1 Gunawardena, Tarini N. A. A1 Ouyang, Hong A1 Eckford, Paul D. W. A1 Gonska, Tanja A1 Moraes, Theo J. A1 Bear, Christine E. PB MDPI AG YR 2020 SN 2075-4426 JF Journal of Personalized Medicine VO 10 IS 4 SP 209 LK http://dx.doi.org/https://doi.org/10.3390/jpm10040209 DO https://doi.org/10.3390/jpm10040209 SF ELIB - SuUB Bremen
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