| 000 | 01655 a2200481 4500 | ||
|---|---|---|---|
| 005 | 20250516151341.0 | ||
| 264 | 0 | _c20131018 | |
| 008 | 201310s 0 0 eng d | ||
| 022 | _a1942-3268 | ||
| 024 | 7 |
_a10.1161/CIRCGENETICS.113.000138 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aBoczek, Nicole J | |
| 245 | 0 | 0 |
_aExome sequencing and systems biology converge to identify novel mutations in the L-type calcium channel, CACNA1C, linked to autosomal dominant long QT syndrome. _h[electronic resource] |
| 260 |
_bCirculation. Cardiovascular genetics _cJun 2013 |
||
| 300 |
_a279-89 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aBase Sequence |
| 650 | 0 | 4 |
_aCalcium Channels, L-Type _xgenetics |
| 650 | 0 | 4 | _aCohort Studies |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 | _aExome |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenes, Dominant |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aLong QT Syndrome _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 | _aMolecular Sequence Data |
| 650 | 0 | 4 | _aMutation, Missense |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aYoung Adult |
| 700 | 1 | _aBest, Jabe M | |
| 700 | 1 | _aTester, David J | |
| 700 | 1 | _aGiudicessi, John R | |
| 700 | 1 | _aMiddha, Sumit | |
| 700 | 1 | _aEvans, Jared M | |
| 700 | 1 | _aKamp, Timothy J | |
| 700 | 1 | _aAckerman, Michael J | |
| 773 | 0 |
_tCirculation. Cardiovascular genetics _gvol. 6 _gno. 3 _gp. 279-89 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1161/CIRCGENETICS.113.000138 _zAvailable from publisher's website |
| 999 |
_c22754969 _d22754969 |
||