Crossmark

Whole-exome sequencing identified a novel heterozygous mutation of SALL1 and a new homozygous mutation of PTPRQ in a Chinese family with Townes-Brocks syndrome and hearing loss

Crossref DOI link: https://doi.org/10.1186/s12920-021-00871-9

Published Online: 2021-01-21

Published Print: 2021-12

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

Authors

Yang, Guangxian http://orcid.org/0000-0002-4473-5127
Yin, Yi

Tan, Zhiping

Liu, Jian

Deng, Xicheng

Yang, Yifeng
License Information

Text and Data Mining valid from 2021-01-21

Version of Record valid from 2021-01-21
More Information

Article History

Received: 27 November 2020

Accepted: 7 January 2021

First Online: 21 January 2021

Change Date: 3 February 2021

Change Type: Update

Change Details: Additional file 2 has been correctly linked.

Ethics approval and consent to participate

: Written informed consent was obtained from all of the adult participants and legal guardians of minor participants. The study was approved by the Ethics Committee of Hunan Children's Hospital (HCHLL-2018-43).

: Written consent was obtained from all the participants or their guardians for the publication of this study.

: The authors declare that they have no competing interests.

Document is current

Any future updates will be listed below