Correction: Nonrandom occurrence of multiple de novo coding variants in a proband indicates the existence of an oligogenic model in autism
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
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| Veröffentlicht in: | Genetics in medicine 2019-11, Vol.21 (11), p.2662-2663 |
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| container_end_page | 2663 |
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| container_issue | 11 |
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| container_title | Genetics in medicine |
| container_volume | 21 |
| creator | Du, Yaoqiang Li, Zhongshan Liu, Zhenwei Zhang, Na Wang, Ruochen Li, Fengxia Zhang, Tao Jiang, Yi Zhi, Xiao Wang, Zhen Wu, Jinyu |
| description | An amendment to this paper has been published and can be accessed via a link at the top of the paper. |
| doi_str_mv | 10.1038/s41436-019-0629-4 |
| format | Article |
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| issn | 1098-3600 1530-0366 |
| language | eng |
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| source | EZB-FREE-00999 freely available EZB journals; ProQuest Central UK/Ireland; Alma/SFX Local Collection |
| subjects | Biomedical and Life Sciences Biomedicine Correction Human Genetics Laboratory Medicine |
| title | Correction: Nonrandom occurrence of multiple de novo coding variants in a proband indicates the existence of an oligogenic model in autism |
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