000 01777 a2200565 4500
005 20250515230251.0
264 0 _c20101202
008 201012s 0 0 eng d
022 _a1942-3268
024 7 _a10.1161/CIRCGENETICS.109.930867
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aLiu, Hui
245 0 0 _aGain-of-function mutations in TRPM4 cause autosomal dominant isolated cardiac conduction disease.
_h[electronic resource]
260 _bCirculation. Cardiovascular genetics
_cAug 2010
300 _a374-85 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAnimals
650 0 4 _aCHO Cells
650 0 4 _aCOS Cells
650 0 4 _aCardiac Conduction System Disease
650 0 4 _aCells, Cultured
650 0 4 _aChlorocebus aethiops
650 0 4 _aCricetinae
650 0 4 _aCricetulus
650 0 4 _aFamily
650 0 4 _aFemale
650 0 4 _aGenes, Dominant
650 0 4 _aGenetic Linkage
650 0 4 _aHeart Block
_xgenetics
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMutation
_xphysiology
650 0 4 _aPedigree
650 0 4 _aTRPM Cation Channels
_xgenetics
650 0 4 _aTransfection
700 1 _aEl Zein, Loubna
700 1 _aKruse, Martin
700 1 _aGuinamard, Romain
700 1 _aBeckmann, Alf
700 1 _aBozio, André
700 1 _aKurtbay, Güven
700 1 _aMégarbané, André
700 1 _aOhmert, Iris
700 1 _aBlaysat, Gérard
700 1 _aVillain, Elisabeth
700 1 _aPongs, Olaf
700 1 _aBouvagnet, Patrice
773 0 _tCirculation. Cardiovascular genetics
_gvol. 3
_gno. 4
_gp. 374-85
856 4 0 _uhttps://doi.org/10.1161/CIRCGENETICS.109.930867
_zAvailable from publisher's website
999 _c19911241
_d19911241