| 000 | 01538 a2200469 4500 | ||
|---|---|---|---|
| 005 | 20250515071048.0 | ||
| 264 | 0 | _c20080225 | |
| 008 | 200802s 0 0 eng d | ||
| 022 | _a0022-2828 | ||
| 024 | 7 |
_a10.1016/j.yjmcc.2007.04.012 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aSaenen, J B | |
| 245 | 0 | 0 |
_aA single hERG mutation underlying a spectrum of acquired and congenital long QT syndrome phenotypes. _h[electronic resource] |
| 260 |
_bJournal of molecular and cellular cardiology _cJul 2007 |
||
| 300 |
_a63-72 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAged |
| 650 | 0 | 4 | _aAmino Acid Sequence |
| 650 | 0 | 4 |
_aAmino Acid Substitution _xgenetics |
| 650 | 0 | 4 | _aBase Sequence |
| 650 | 0 | 4 | _aCanada |
| 650 | 0 | 4 | _aCell Line |
| 650 | 0 | 4 |
_aEther-A-Go-Go Potassium Channels _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Diseases, Inborn |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aLong QT Syndrome _xgenetics |
| 650 | 0 | 4 | _aNetherlands |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPoint Mutation |
| 650 | 0 | 4 | _aWhite People |
| 700 | 1 | _aPaulussen, A D C | |
| 700 | 1 | _aJongbloed, R J | |
| 700 | 1 | _aMarcelis, C L | |
| 700 | 1 | _aGilissen, R A H J | |
| 700 | 1 | _aAerssens, J | |
| 700 | 1 | _aSnyders, D J | |
| 700 | 1 | _aRaes, A L | |
| 773 | 0 |
_tJournal of molecular and cellular cardiology _gvol. 43 _gno. 1 _gp. 63-72 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.yjmcc.2007.04.012 _zAvailable from publisher's website |
| 999 |
_c17071745 _d17071745 |
||