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 |