| 000 | 01627 a2200505 4500 | ||
|---|---|---|---|
| 005 | 20250518031957.0 | ||
| 264 | 0 | _c20190820 | |
| 008 | 201908s 0 0 eng d | ||
| 022 | _a1471-2350 | ||
| 024 | 7 |
_a10.1186/s12881-019-0788-9 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aLiao, Xin | |
| 245 | 0 | 0 |
_aRare RNF213 variants and the risk of intracranial artery stenosis/occlusion disease in Chinese population: a case-control study. _h[electronic resource] |
| 260 |
_bBMC medical genetics _c03 2019 |
||
| 300 |
_a55 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aAdenosine Triphosphatases _xgenetics |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aAged |
| 650 | 0 | 4 |
_aAsian People _xgenetics |
| 650 | 0 | 4 | _aCase-Control Studies |
| 650 | 0 | 4 | _aChina |
| 650 | 0 | 4 | _aExome |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Testing |
| 650 | 0 | 4 | _aGenetic Variation |
| 650 | 0 | 4 | _aHeterozygote |
| 650 | 0 | 4 |
_aHigh-Throughput Nucleotide Sequencing _xmethods |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aSequence Analysis, DNA _xmethods |
| 650 | 0 | 4 |
_aUbiquitin-Protein Ligases _xgenetics |
| 650 | 0 | 4 |
_aVertebrobasilar Insufficiency _xgenetics |
| 700 | 1 | _aZhang, Tong | |
| 700 | 1 | _aLi, Bingyang | |
| 700 | 1 | _aHu, Shimin | |
| 700 | 1 | _aLiu, Junyu | |
| 700 | 1 | _aDeng, Jing | |
| 700 | 1 | _aTan, Hongzhuan | |
| 700 | 1 | _aYan, Junxia | |
| 773 | 0 |
_tBMC medical genetics _gvol. 20 _gno. 1 _gp. 55 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1186/s12881-019-0788-9 _zAvailable from publisher's website |
| 999 |
_c29530820 _d29530820 |
||