000 01545 a2200433 4500
005 20250514050904.0
264 0 _c20030103
008 200301s 0 0 eng d
022 _a1098-1004
024 7 _a10.1002/humu.10131
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aJongbloed, Roselie
245 0 0 _aDHPLC analysis of potassium ion channel genes in congenital long QT syndrome.
_h[electronic resource]
260 _bHuman mutation
_cNov 2002
300 _a382-91 p.
_bdigital
500 _aPublication Type: Evaluation Study; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aBase Sequence
650 0 4 _aCation Transport Proteins
650 0 4 _aChromatography, High Pressure Liquid
_xmethods
650 0 4 _aDNA Mutational Analysis
_xmethods
650 0 4 _aEther-A-Go-Go Potassium Channels
650 0 4 _aKCNQ Potassium Channels
650 0 4 _aKCNQ1 Potassium Channel
650 0 4 _aLong QT Syndrome
_xgenetics
650 0 4 _aMolecular Sequence Data
650 0 4 _aMutation
650 0 4 _aNucleic Acid Denaturation
650 0 4 _aPolymerase Chain Reaction
650 0 4 _aPolymorphism, Single Nucleotide
650 0 4 _aPotassium Channels
_xgenetics
650 0 4 _aPotassium Channels, Voltage-Gated
700 1 _aMarcelis, Carlo
700 1 _aVelter, Crool
700 1 _aDoevendans, Pieter
700 1 _aGeraedts, Joep
700 1 _aSmeets, Hubert
773 0 _tHuman mutation
_gvol. 20
_gno. 5
_gp. 382-91
856 4 0 _uhttps://doi.org/10.1002/humu.10131
_zAvailable from publisher's website
999 _c12210835
_d12210835