000			02034 a2200589 4500
005			20250515173223.0
264		0	_c20100426
008			201004s 0 0 eng d
022			_a1540-8167
024	7		_a10.1111/j.1540-8167.2009.01468.x _2doi
040			_aNLM _beng _cNLM
100	1		_aZhao, Jing Ting
245	0	0	_aNot all hERG pore domain mutations have a severe phenotype: G584S has an inactivation gating defect with mild phenotype compared to G572S, which has a dominant negative trafficking defect and a severe phenotype. _h[electronic resource]
260			_bJournal of cardiovascular electrophysiology _cAug 2009
300			_a923-30 p. _bdigital
500			_aPublication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
650	0	4	_aAdolescent
650	0	4	_aAdult
650	0	4	_aAmino Acid Sequence
650	0	4	_aAnimals
650	0	4	_aCHO Cells
650	0	4	_aCell Line
650	0	4	_aChild
650	0	4	_aCricetinae
650	0	4	_aCricetulus
650	0	4	_aERG1 Potassium Channel
650	0	4	_aEther-A-Go-Go Potassium Channels _xantagonists & inhibitors
650	0	4	_aFemale
650	0	4	_aGene Silencing
650	0	4	_aHumans
650	0	4	_aMale
650	0	4	_aMiddle Aged
650	0	4	_aMolecular Sequence Data
650	0	4	_aMutation _xgenetics
650	0	4	_aPedigree
650	0	4	_aPhenotype
650	0	4	_aProtein Structure, Tertiary _xgenetics
650	0	4	_aProtein Transport _xgenetics
650	0	4	_aSeverity of Illness Index
650	0	4	_aYoung Adult
700	1		_aHill, Adam P
700	1		_aVarghese, Anthony
700	1		_aCooper, Antony A
700	1		_aSwan, Heikki
700	1		_aLaitinen-Forsblom, Päivi J
700	1		_aRees, Mark I
700	1		_aSkinner, Jonathan R
700	1		_aCampbell, Terence J
700	1		_aVandenberg, Jamie I
773	0		_tJournal of cardiovascular electrophysiology _gvol. 20 _gno. 8 _gp. 923-30
856	4	0	_uhttps://doi.org/10.1111/j.1540-8167.2009.01468.x _zAvailable from publisher's website
999			_c18914908 _d18914908