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 |