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F1099L-CFTR (c.3297C>G) has Impaired Channel Function and Associates with Mild Disease Phenotypes in Two Pediatric Patients.
Life (Basel). 2021 Feb 8;11(2):131. doi: 10.3390/life11020131.
Life (Basel). 2021.
PMID: 33567498
Free PMC article.
c.3623G > A mutation encodes a CFTR protein with impaired channel function.
Zhang X, Hothi JS, Zhang YH, Srinivasan S, Stokes DC, Zhang W.
Zhang X, et al. Among authors: hothi js.
Respir Res. 2016 Jan 22;17:8. doi: 10.1186/s12931-016-0326-7.
Respir Res. 2016.
PMID: 26800689
Free PMC article.
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