| 000 | 01593 a2200469 4500 | ||
|---|---|---|---|
| 005 | 20250517232952.0 | ||
| 264 | 0 | _c20180824 | |
| 008 | 201808s 0 0 eng d | ||
| 022 | _a1536-5964 | ||
| 024 | 7 |
_a10.1097/MD.0000000000011865 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aNandakumar, Priyanka | |
| 245 | 0 | 0 |
_aContributions of rare coding variants in hypotension syndrome genes to population blood pressure variation. _h[electronic resource] |
| 260 |
_bMedicine _cAug 2018 |
||
| 300 |
_ae11865 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 |
_aBlack People _xgenetics |
| 650 | 0 | 4 |
_aBlood Pressure _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Predisposition to Disease |
| 650 | 0 | 4 | _aGenetic Variation |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aHypertension _xgenetics |
| 650 | 0 | 4 |
_aHypotension _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aPotassium Channels, Inwardly Rectifying _xgenetics |
| 650 | 0 | 4 | _aProspective Studies |
| 650 | 0 | 4 | _aReproducibility of Results |
| 650 | 0 | 4 | _aRisk Factors |
| 650 | 0 | 4 |
_aSolute Carrier Family 12, Member 1 _xgenetics |
| 650 | 0 | 4 |
_aSolute Carrier Family 12, Member 3 _xgenetics |
| 650 | 0 | 4 |
_aWhite People _xgenetics |
| 650 | 0 | 4 | _aExome Sequencing |
| 700 | 1 | _aMorrison, Alanna C | |
| 700 | 1 | _aGrove, Megan L | |
| 700 | 1 | _aBoerwinkle, Eric | |
| 700 | 1 | _aChakravarti, Aravinda | |
| 773 | 0 |
_tMedicine _gvol. 97 _gno. 33 _gp. e11865 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1097/MD.0000000000011865 _zAvailable from publisher's website |
| 999 |
_c28735576 _d28735576 |
||