| 000 | 01631 a2200517 4500 | ||
|---|---|---|---|
| 005 | 20250517003313.0 | ||
| 264 | 0 | _c20150730 | |
| 008 | 201507s 0 0 eng d | ||
| 022 | _a2041-1723 | ||
| 024 | 7 |
_a10.1038/ncomms6595 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aO'Roak, B J | |
| 245 | 0 | 0 |
_aRecurrent de novo mutations implicate novel genes underlying simplex autism risk. _h[electronic resource] |
| 260 |
_bNature communications _cNov 2014 |
||
| 300 |
_a5595 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aAutistic Disorder _xgenetics |
| 650 | 0 | 4 | _aBase Sequence |
| 650 | 0 | 4 |
_aCarrier Proteins _xgenetics |
| 650 | 0 | 4 |
_aDNA-Binding Proteins _xgenetics |
| 650 | 0 | 4 | _aFamily |
| 650 | 0 | 4 | _aGenetic Predisposition to Disease |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aIntelligence _xgenetics |
| 650 | 0 | 4 | _aIntelligence Tests |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aPAX5 Transcription Factor _xgenetics |
| 650 | 0 | 4 | _aRisk |
| 650 | 0 | 4 | _aSequence Analysis, DNA |
| 650 | 0 | 4 |
_aUbiquitin-Protein Ligases _xgenetics |
| 650 | 0 | 4 |
_aras GTPase-Activating Proteins _xgenetics |
| 700 | 1 | _aStessman, H A | |
| 700 | 1 | _aBoyle, E A | |
| 700 | 1 | _aWitherspoon, K T | |
| 700 | 1 | _aMartin, B | |
| 700 | 1 | _aLee, C | |
| 700 | 1 | _aVives, L | |
| 700 | 1 | _aBaker, C | |
| 700 | 1 | _aHiatt, J B | |
| 700 | 1 | _aNickerson, D A | |
| 700 | 1 | _aBernier, R | |
| 700 | 1 | _aShendure, J | |
| 700 | 1 | _aEichler, E E | |
| 773 | 0 |
_tNature communications _gvol. 5 _gp. 5595 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1038/ncomms6595 _zAvailable from publisher's website |
| 999 |
_c24374299 _d24374299 |
||