| 000 | 01695 a2200565 4500 | ||
|---|---|---|---|
| 005 | 20250514074328.0 | ||
| 264 | 0 | _c20040105 | |
| 008 | 200401s 0 0 eng d | ||
| 022 | _a0364-5134 | ||
| 024 | 7 |
_a10.1002/ana.10607 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aChen, Yucai | |
| 245 | 0 | 0 |
_aAssociation between genetic variation of CACNA1H and childhood absence epilepsy. _h[electronic resource] |
| 260 |
_bAnnals of neurology _cAug 2003 |
||
| 300 |
_a239-43 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAge of Onset |
| 650 | 0 | 4 | _aAmino Acid Substitution |
| 650 | 0 | 4 |
_aCalcium Channels, T-Type _xgenetics |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aChina |
| 650 | 0 | 4 |
_aDNA _xgenetics |
| 650 | 0 | 4 | _aElectroencephalography |
| 650 | 0 | 4 |
_aEpilepsy, Absence _xgenetics |
| 650 | 0 | 4 |
_aExons _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Variation |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMutation, Missense _xgenetics |
| 650 | 0 | 4 | _aReverse Transcriptase Polymerase Chain Reaction |
| 700 | 1 | _aLu, Jianjun | |
| 700 | 1 | _aPan, Hong | |
| 700 | 1 | _aZhang, Yuehua | |
| 700 | 1 | _aWu, Husheng | |
| 700 | 1 | _aXu, Keming | |
| 700 | 1 | _aLiu, Xiaoyan | |
| 700 | 1 | _aJiang, Yuwu | |
| 700 | 1 | _aBao, Xinhua | |
| 700 | 1 | _aYao, Zhijian | |
| 700 | 1 | _aDing, Keyue | |
| 700 | 1 | _aLo, Wilson H Y | |
| 700 | 1 | _aQiang, Boqin | |
| 700 | 1 | _aChan, Piu | |
| 700 | 1 | _aShen, Yan | |
| 700 | 1 | _aWu, Xiru | |
| 773 | 0 |
_tAnnals of neurology _gvol. 54 _gno. 2 _gp. 239-43 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/ana.10607 _zAvailable from publisher's website |
| 999 |
_c12668302 _d12668302 |
||