| 000 | 01729 a2200517 4500 | ||
|---|---|---|---|
| 005 | 20250516002719.0 | ||
| 264 | 0 | _c20110524 | |
| 008 | 201105s 0 0 eng d | ||
| 022 | _a1556-3871 | ||
| 024 | 7 |
_a10.1016/j.hrthm.2010.09.010 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aBartos, Daniel C | |
| 245 | 0 | 0 |
_aR231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation. _h[electronic resource] |
| 260 |
_bHeart rhythm _cJan 2011 |
||
| 300 |
_a48-55 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 |
_aAtrial Fibrillation _xgenetics |
| 650 | 0 | 4 | _aComputational Biology |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aGenetic Pleiotropy _xgenetics |
| 650 | 0 | 4 |
_aGenetic Predisposition to Disease _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aKCNQ1 Potassium Channel _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMutation, Missense |
| 650 | 0 | 4 | _aPatch-Clamp Techniques |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
| 650 | 0 | 4 |
_aRomano-Ward Syndrome _xgenetics |
| 700 | 1 | _aDuchatelet, Sabine | |
| 700 | 1 | _aBurgess, Don E | |
| 700 | 1 | _aKlug, Didier | |
| 700 | 1 | _aDenjoy, Isabelle | |
| 700 | 1 | _aPeat, Rachel | |
| 700 | 1 | _aLupoglazoff, Jean-Marc | |
| 700 | 1 | _aFressart, Véronique | |
| 700 | 1 | _aBerthet, Myriam | |
| 700 | 1 | _aAckerman, Michael J | |
| 700 | 1 | _aJanuary, Craig T | |
| 700 | 1 | _aGuicheney, Pascale | |
| 700 | 1 | _aDelisle, Brian P | |
| 773 | 0 |
_tHeart rhythm _gvol. 8 _gno. 1 _gp. 48-55 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.hrthm.2010.09.010 _zAvailable from publisher's website |
| 999 |
_c20180946 _d20180946 |
||