PUBLICATION
CORRECTION: Rare coding variants in MAPK7 predispose to adolescent idiopathic scoliosis
- Authors
- Gao, W., Chen, C., Zhou, T., Yang, S., Gao, B., Zhou, H., Lian, C., Wu, Z., Qiu, X., Yang, X., Alattar, E., Liu, W., Su, D., Sun, S., Chen, Y., Cheung, K.M.C., Song, Y., Luk, K.K.D., Chan, D., Sham, P.C., Xing, C., Khor, C.C., Liu, G., Yang, J., Deng, Y., Hao, D., Huang, D., Li, Q.Z., Xu, C., Su, P.
- ID
- ZDB-PUB-220906-233
- Date
- 2021
- Source
- Human Mutation 42: 218 (Other)
- Registered Authors
- Keywords
- none
- MeSH Terms
- none
- PubMed
- 33559989 Full text @ Hum. Mutat.
Citation
Gao, W., Chen, C., Zhou, T., Yang, S., Gao, B., Zhou, H., Lian, C., Wu, Z., Qiu, X., Yang, X., Alattar, E., Liu, W., Su, D., Sun, S., Chen, Y., Cheung, K.M.C., Song, Y., Luk, K.K.D., Chan, D., Sham, P.C., Xing, C., Khor, C.C., Liu, G., Yang, J., Deng, Y., Hao, D., Huang, D., Li, Q.Z., Xu, C., Su, P. (2021) CORRECTION: Rare coding variants in MAPK7 predispose to adolescent idiopathic scoliosis. Human Mutation. 42:218.
Abstract
In (Gao et al., 2017), Caixia Xu is a co-corresponding author with below details. She had been mistakenly listed as a co-author and we′re correcting the error with release of a corrigendum.
Caixia Xu3*
3 Research Centre for Translational Medicine, First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China
*Correspondence: Caixia Xu, Research Centre for Translational Medicine, First Affiliated Hospital, Sun Yat-Sen University, No. 58 Zhongshan 2nd Road, Yuexiu District, Guangzhou 510080, China. Email: xucx3@mail.sysu.edu.cn
Authors apologize for the error.
Errata / Notes
This article corrects ZDB-PUB-170718-5 .
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping