| 000 | 01137 a2200301 4500 | ||
|---|---|---|---|
| 005 | 20250513100257.0 | ||
| 264 | 0 | _c19961028 | |
| 008 | 199610s 0 0 eng d | ||
| 022 | _a1357-4310 | ||
| 024 | 7 |
_a10.1016/1357-4310(96)10028-9 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aSheppard, D N | |
| 245 | 0 | 0 |
_aUnderstanding how cystic fibrosis mutations cause a loss of Cl- channel function. _h[electronic resource] |
| 260 |
_bMolecular medicine today _cJul 1996 |
||
| 300 |
_a290-7 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Review | ||
| 650 | 0 | 4 |
_aChlorides _xmetabolism |
| 650 | 0 | 4 |
_aCystic Fibrosis _xgenetics |
| 650 | 0 | 4 |
_aCystic Fibrosis Transmembrane Conductance Regulator _xgenetics |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aModels, Molecular |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aPatch-Clamp Techniques |
| 700 | 1 | _aOstedgaard, L S | |
| 773 | 0 |
_tMolecular medicine today _gvol. 2 _gno. 7 _gp. 290-7 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/1357-4310(96)10028-9 _zAvailable from publisher's website |
| 999 |
_c8793225 _d8793225 |
||