000 01426 a2200397 4500
005 20250514025301.0
264 0 _c20020327
008 200203s 0 0 eng d
022 _a0002-9343
024 7 _a10.1016/s0002-9343(01)01136-6
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aWarnock, David G
245 0 0 _aGenetic forms of renal potassium and magnesium wasting.
_h[electronic resource]
260 _bThe American journal of medicine
_cFeb 2002
300 _a235-6 p.
_bdigital
500 _aPublication Type: Comment; Editorial
650 0 4 _aBartter Syndrome
_xgenetics
650 0 4 _aCarrier Proteins
_xgenetics
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aHypokalemia
_xgenetics
650 0 4 _aMagnesium Deficiency
_xgenetics
650 0 4 _aMutation
650 0 4 _aPhenotype
650 0 4 _aPotassium Channels
_xgenetics
650 0 4 _aPotassium Channels, Inwardly Rectifying
650 0 4 _aReceptors, Drug
650 0 4 _aRenal Tubular Transport, Inborn Errors
_xgenetics
650 0 4 _aSodium Chloride Symporters
650 0 4 _aSodium-Potassium-Chloride Symporters
_xgenetics
650 0 4 _aSolute Carrier Family 12, Member 1
650 0 4 _aSolute Carrier Family 12, Member 3
650 0 4 _aSymporters
773 0 _tThe American journal of medicine
_gvol. 112
_gno. 3
_gp. 235-6
856 4 0 _uhttps://doi.org/10.1016/s0002-9343(01)01136-6
_zAvailable from publisher's website
999 _c11799827
_d11799827