De novo mutations in PLXND1 and REV3L cause Möbius syndrome.
dc.contributor.author | SORIA, L | |
dc.contributor.author | van, Beusekom | |
dc.contributor.author | ROSCIOLI, T | |
dc.contributor.author | IQBAL, Z | |
dc.contributor.author | GILISSEN, C | |
dc.contributor.author | HOISCHEN, A | |
dc.contributor.author | de, Brouwer | |
dc.contributor.author | ERASMUS, C | |
dc.contributor.author | SCHUBERT, D | |
dc.contributor.author | BRUNNER, H | |
dc.contributor.author | Pérez, Aytés | |
dc.contributor.author | MARIN, F | |
dc.contributor.author | TOMAS-ROCA, L | |
dc.contributor.author | AROCA, P | |
dc.contributor.author | KAYSERILI, H | |
dc.contributor.author | CARTA, A | |
dc.contributor.author | de, Wind | |
dc.contributor.author | PADBERG, GW | |
dc.contributor.author | van, Bokhoven | |
dc.contributor.author | Altunoglu, UMUT | |
dc.contributor.author | TSAALBI-SHTYLIK, A | |
dc.contributor.author | JANSEN, JG | |
dc.contributor.author | SINGH, MK | |
dc.contributor.author | EPSTEIN, JA | |
dc.contributor.author | VERZIJL, H | |
dc.date.accessioned | 2021-03-03T17:52:22Z | |
dc.date.available | 2021-03-03T17:52:22Z | |
dc.identifier.citation | TOMAS-ROCA L., TSAALBI-SHTYLIK A., JANSEN J., SINGH M., EPSTEIN J., Altunoglu U., VERZIJL H., SORIA L., van B., ROSCIOLI T., et al., "De novo mutations in PLXND1 and REV3L cause Möbius syndrome.", Nature communications, cilt.6, ss.7199, 2015 | |
dc.identifier.issn | 2041-1723 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_4bedb2b0-cf60-49b8-96e4-5211c08acc3e | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/54440 | |
dc.identifier.uri | https://doi.org/10.1038/ncomms8199 | |
dc.language.iso | eng | |
dc.title | De novo mutations in PLXND1 and REV3L cause Möbius syndrome. | |
dc.type | Makale | |
dc.relation.journal | Nature communications | |
dc.contributor.department | , , | |
dc.identifier.volume | 6 | |
dc.identifier.startpage | 7199 | |
dc.identifier.endpage | 7199 | |
dc.contributor.firstauthorID | 182068 |
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