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A novel deletion mutation of the SOX2 gene in a child of Chinese origin with congenital bilateral anophthalmia and sensorineural hearing loss

Crossref DOI link: https://doi.org/10.1007/s12041-018-0970-4

Published Online: 2018-08-18

Published Print: 2018-09

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

Authors

Zhang, Yan

Zhang, Xibo

Long, Ran

Yu, Ling https://orcid.org/0000-0002-1931-2800
Funding

Funding for this research was provided by:

National Natural Science Foundation of China (No. 81570841)

Southwest Medical University Affiliated Hospital Foundation (No. 16004)
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Article History

Received: 31 July 2017

Revised: 17 November 2017

Accepted: 16 January 2018

First Online: 18 August 2018