000 01040 a2200265 4500
005 20250518032402.0
264 0 _c20190703
008 201907s 0 0 eng d
022 _a1535-4970
024 7 _a10.1164/rccm.201903-0696ED
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aZemanick, Edith T
245 0 0 _aUnraveling the CFTR Function-Phenotype Connection for Precision Treatment in Cystic Fibrosis.
_h[electronic resource]
260 _bAmerican journal of respiratory and critical care medicine
_cMay 2019
300 _a1053-1054 p.
_bdigital
500 _aPublication Type: Journal Article; Comment
650 0 4 _aCystic Fibrosis
650 0 4 _aCystic Fibrosis Transmembrane Conductance Regulator
_xgenetics
650 0 4 _aHumans
650 0 4 _aMutation
650 0 4 _aPhenotype
700 1 _aPolineni, Deepika
773 0 _tAmerican journal of respiratory and critical care medicine
_gvol. 199
_gno. 9
_gp. 1053-1054
856 4 0 _uhttps://doi.org/10.1164/rccm.201903-0696ED
_zAvailable from publisher's website
999 _c29543942
_d29543942