Correction: Nonrandom occurrence of multiple de novo coding variants in a proband indicates the existence of an oligogenic model in autism.

Du, Yaoqiang; Li, Zhongshan; Liu, Zhenwei; Zhang, Na; Wang, Ruochen; Li, Fengxia; Zhang, Tao; Jiang, Yi; Zhi, Xiao; Wang, Zhen; Wu, Jinyu.

Afiliação

Du Y; Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, China.
Li Z; Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, China.
Liu Z; Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, China.
Zhang N; Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, China.
Wang R; Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, China.
Li F; Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, China.
Zhang T; Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, China.
Jiang Y; Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, China.
Zhi X; Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, China.
Wang Z; Research Center of Blood Transfusion Medicine, Education Ministry Key Laboratory of Laboratory Medicine, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College, Hangzhou, China.
Wu J; Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, China. iamwujy@gmail.com.

Genet Med ; 21(11): 2662-2663, 2019 11.

Article em En | MEDLINE | ID: mdl-31367017

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article