000			01260 a2200313 4500
005			20250515002252.0
264		0	_c20060213
008			200602s 0 0 eng d
022			_a1547-5271
024	7		_a10.1016/j.hrthm.2005.07.024 _2doi
040			_aNLM _beng _cNLM
100	1		_aAnderson, Mark E
245	0	0	_a"We are not alone": ion channel mutations in a long QT syndrome cohort. _h[electronic resource]
260			_bHeart rhythm _cOct 2005
300			_a1106-7 p. _bdigital
500			_aPublication Type: Comment; Editorial; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
650	0	4	_aCohort Studies
650	0	4	_aGenetic Predisposition to Disease _xgenetics
650	0	4	_aGenetic Testing
650	0	4	_aHumans
650	0	4	_aLong QT Syndrome _xdiagnosis
650	0	4	_aMutation, Missense _xgenetics
650	0	4	_aPolymorphism, Genetic _xgenetics
650	0	4	_aRyanodine Receptor Calcium Release Channel _xgenetics
650	0	4	_aTachycardia, Ventricular _xgenetics
650	0	4	_aVentricular Fibrillation _xgenetics
773	0		_tHeart rhythm _gvol. 2 _gno. 10 _gp. 1106-7
856	4	0	_uhttps://doi.org/10.1016/j.hrthm.2005.07.024 _zAvailable from publisher's website
999			_c15819841 _d15819841