| 000 | 01891 a2200649 4500 | ||
|---|---|---|---|
| 005 | 20250516210720.0 | ||
| 264 | 0 | _c20140813 | |
| 008 | 201408s 0 0 eng d | ||
| 022 | _a1476-4687 | ||
| 024 | 7 |
_a10.1038/nature13127 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aMacArthur, D G | |
| 245 | 0 | 0 |
_aGuidelines for investigating causality of sequence variants in human disease. _h[electronic resource] |
| 260 |
_bNature _cApr 2014 |
||
| 300 |
_a469-76 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 | _aDisease |
| 650 | 0 | 4 | _aFalse Positive Reactions |
| 650 | 0 | 4 |
_aGenes _xgenetics |
| 650 | 0 | 4 |
_aGenetic Predisposition to Disease _xgenetics |
| 650 | 0 | 4 |
_aGenetic Variation _xgenetics |
| 650 | 0 | 4 | _aGuidelines as Topic |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInformation Dissemination |
| 650 | 0 | 4 | _aPublishing |
| 650 | 0 | 4 | _aReproducibility of Results |
| 650 | 0 | 4 | _aResearch Design |
| 650 | 0 | 4 |
_aTranslational Research, Biomedical _xstandards |
| 700 | 1 | _aManolio, T A | |
| 700 | 1 | _aDimmock, D P | |
| 700 | 1 | _aRehm, H L | |
| 700 | 1 | _aShendure, J | |
| 700 | 1 | _aAbecasis, G R | |
| 700 | 1 | _aAdams, D R | |
| 700 | 1 | _aAltman, R B | |
| 700 | 1 | _aAntonarakis, S E | |
| 700 | 1 | _aAshley, E A | |
| 700 | 1 | _aBarrett, J C | |
| 700 | 1 | _aBiesecker, L G | |
| 700 | 1 | _aConrad, D F | |
| 700 | 1 | _aCooper, G M | |
| 700 | 1 | _aCox, N J | |
| 700 | 1 | _aDaly, M J | |
| 700 | 1 | _aGerstein, M B | |
| 700 | 1 | _aGoldstein, D B | |
| 700 | 1 | _aHirschhorn, J N | |
| 700 | 1 | _aLeal, S M | |
| 700 | 1 | _aPennacchio, L A | |
| 700 | 1 | _aStamatoyannopoulos, J A | |
| 700 | 1 | _aSunyaev, S R | |
| 700 | 1 | _aValle, D | |
| 700 | 1 | _aVoight, B F | |
| 700 | 1 | _aWinckler, W | |
| 700 | 1 | _aGunter, C | |
| 773 | 0 |
_tNature _gvol. 508 _gno. 7497 _gp. 469-76 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1038/nature13127 _zAvailable from publisher's website |
| 999 |
_c23762920 _d23762920 |
||