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作者更正：累积单基因功能丧失变异导致神经管缺陷风险的阈值

Author Correction: Threshold for neural tube defect risk by accumulated singleton loss-of-function variants.

作者信息

Chen Zhongzhong, Lei Yunping, Zheng Yufang, Aguiar-Pulido Vanessa, Ross M Elizabeth, Peng Rui, Jin Li, Zhang Ting, Finnell Richard H, Wang Hongyan

机构信息

Obstetrics and Gynecology Hospital, State Key Laboratory of Genetic Engineering at School of Life Sciences, Institute of Reproduction and Development, Fudan University, Shanghai, 200011, China.

Key Laboratory of Reproduction Regulation of NPFPC, Collaborative Innovation Center of Genetics and Development, Fudan University, Shanghai, 200032, China.

出版信息

Cell Res. 2019 Sep;29(9):776. doi: 10.1038/s41422-019-0201-4.

DOI:10.1038/s41422-019-0201-4
PMID:31346254
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6796949/
Abstract

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

摘要

本文的一个修订版本已发表，可通过本文顶部的链接获取。

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Neonatal ten-year retrospective study on neural tube defects in a second level University Hospital.二级大学医院神经管缺陷的十年回顾性研究。
Ital J Pediatr. 2020 May 24;46(1):72. doi: 10.1186/s13052-020-00836-1.