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Addition of an affected family member to a previously ascertained autosomal recessive nonsyndromic hearing loss pedigree and systematic phenotype-genotype analysis of splice-site variants in MYO15A

Crossref DOI link: https://doi.org/10.1186/s12920-022-01368-9

Published Online: 2022-11-18

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

Authors

Yang, Jin-Yuan

Wang, Wei-Qian

Han, Ming-Yu

Huang, Sha-Sha

Wang, Guo-Jian

Su, Yu

Xu, Jin-Cao

Fu, Ying

Kang, Dong-Yang

Yang, Kun

Zhang, Xin

Liu, Xing

Gao, Xue

Yuan, Yong-Yi

Dai, Pu
Funding

Funding for this research was provided by:

National Natural Science Foundation of China (81900953, 82171158, 81873704)

Natural Science Foundation of Hainan Province (819MS110)
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Text and Data Mining valid from 2022-11-18

Version of Record valid from 2022-11-18
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Article History

Received: 17 June 2022

Accepted: 29 September 2022

First Online: 18 November 2022

Declarations

:

: This study was approved by the Chinese PLA General Hospital Research Ethics Committee. Parents of minor subject (5 year-old) signed informed consent forms for participation in clinical and genetic research. In this study, all methods were performed in accordance with the relevant guidelines and regulations.

: We obtained fully informed written consent from parents of minor subjects for publication of their clinical data.

: The authors declare that there is no competing interest in this research.

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