Correction: Nonrandom occurrence of multiple de novo coding variants in a proband indicates the existence of an oligogenic model in autism (Genetics in Medicine, (2019), 10.1038/s41436-019-0610-2)

doi:10.1038/s41436-019-0629-4

科研成果详情

名称	Correction: Nonrandom occurrence of multiple de novo coding variants in a proband indicates the existence of an oligogenic model in autism (Genetics in Medicine, (2019), 10.1038/s41436-019-0610-2)
作者	Du, Yaoqiang 1; Li, Zhongshan1; Liu, Zhenwei1; Zhang, Na 1; Wang, Ruochen1; Li, Fengxia 1; Zhang, Tao 1; Jiang, Yi 1; Zhi, Xiao 1; Wang, Zhen 2; Wu, Jinyu 1
发表期刊	Genetics in Medicine;
语种	英语
原始文献类型	Erratum
摘要	In the original version of the published Article the word “mutation” was used throughout the text. The ACMG changed its terminology from “mutation” to “variant” prior to the publication of the Article and the requested text changes were not incorporated by the typesetter. The PDF and HTML versions of the Article have now been modified accordingly.
出版者	NATURE PUBLISHING GROUP
ISSN	1098-3600
EISSN	1530-0366
卷号	21
期号	11
页码	2662-2663
DOI	10.1038/s41436-019-0629-4
页数	1
WOS类目	Genetics & Heredity
WOS研究方向	Genetics & Heredity
WOS记录号	WOS:000494989200036
收录类别	SCOPUS ; SCIE ; SSCI
发布日期	2019-11-01
URL	查看原文
PubMed ID	31367017
通讯作者地址	[Wu, Jinyu]Wenzhou Med Univ, Inst Genom Med, Wenzhou, Peoples R China.
Scopus学科分类	Genetics (clinical)
SCOPUSEID	2-s2.0-85069947056
TOP期刊	TOP期刊
引用统计
文献类型	其他
条目标识符	https://kms.wmu.edu.cn/handle/3ETUA0LF/185545
专题	基因组医学研究院
通讯作者	Wu, Jinyu
作者单位	1.Wenzhou Med Univ, Inst Genom Med, Wenzhou, Peoples R China; 2.Hangzhou Med Coll, Zhejiang Prov Peoples Hosp, Res Ctr Blood Transfus Med, Educ Minist,Key Lab Lab Med,Peoples Hosp, Hangzhou, Zhejiang, Peoples R China
第一作者单位	基因组医学研究院
通讯作者单位	基因组医学研究院
推荐引用方式 GB/T 7714	Du, Yaoqiang,Li, Zhongshan,Liu, Zhenwei,et al. Correction: Nonrandom occurrence of multiple de novo coding variants in a proband indicates the existence of an oligogenic model in autism (Genetics in Medicine, (2019), 10.1038/s41436-019-0610-2). 2019.