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De novo ATP1A2 variants in two Chinese children with alternating hemiplegia of childhood upgraded the gene–disease relationship and variant classification: a case report

Crossref DOI link: https://doi.org/10.1186/s12920-021-00947-6

Published Online: 2021-04-01

Published Print: 2021-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Huang, Danping

Liu, Min

Wang, Hongying

Zhang, Bingbing

Zhao, Dongjing

Ling, Weihao

Wang, Manli

Feng, Jun

Shen, Yiping

Chen, Xuqin
Funding

Funding for this research was provided by:

the Key special program funds of Jiangsu Province (BE2018661)

Special project of diagnosis and treatment technology for key clinical diseases in Suzhou (LCZX201810)

the 15th batch of six talent peak training funds in Jiangsu Province (WSN-028)
License Information

Text and Data Mining valid from 2021-04-01

Version of Record valid from 2021-04-01
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Article History

Received: 19 November 2020

Accepted: 25 March 2021

First Online: 1 April 2021

Declarations

:

: This study was approved by the Ethics Committee of the Children’s Hospital of Soochow University. Written informed consent was obtained from both of the parents of each of the patients to participate in our study.

: Written informed consent was obtained from both of the parents of each of the patients for publication of this case report and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.

: The authors declare that they have no competing interests.

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