000			01631 a2200493 4500
005			20250513101711.0
264		0	_c19961112
008			199611s 0 0 eng d
022			_a1061-4036
024	7		_a10.1038/ng1096-152 _2doi
040			_aNLM _beng _cNLM
100	1		_aSimon, D B
245	0	0	_aGenetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK. _h[electronic resource]
260			_bNature genetics _cOct 1996
300			_a152-6 p. _bdigital
500			_aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
650	0	4	_aAmino Acid Sequence
650	0	4	_aBartter Syndrome _xgenetics
650	0	4	_aCarrier Proteins _xgenetics
650	0	4	_aCell Membrane _xchemistry
650	0	4	_aConsanguinity
650	0	4	_aConserved Sequence
650	0	4	_aDNA Mutational Analysis
650	0	4	_aFemale
650	0	4	_aGenetic Heterogeneity
650	0	4	_aGenotype
650	0	4	_aHumans
650	0	4	_aMale
650	0	4	_aMutation
650	0	4	_aPedigree
650	0	4	_aPolymorphism, Single-Stranded Conformational
650	0	4	_aPotassium Channels _xchemistry
650	0	4	_aPotassium Channels, Inwardly Rectifying
650	0	4	_aSodium-Potassium-Chloride Symporters
700	1		_aKaret, F E
700	1		_aRodriguez-Soriano, J
700	1		_aHamdan, J H
700	1		_aDiPietro, A
700	1		_aTrachtman, H
700	1		_aSanjad, S A
700	1		_aLifton, R P
773	0		_tNature genetics _gvol. 14 _gno. 2 _gp. 152-6
856	4	0	_uhttps://doi.org/10.1038/ng1096-152 _zAvailable from publisher's website
999			_c8835371 _d8835371