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Diagnosis of a patient with severe sensorineural hearing loss as the initial symptom caused by novel compound heterozygous variant in SLC19A2 gene

Crossref DOI link: https://doi.org/10.1016/j.bjorl.2025.101581

Published Print: 2025-07

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Shi, Yanan https://orcid.org/0009-0007-3876-1226
Li, Junyang https://orcid.org/0000-0002-7402-4473
Chen, Xiaoqin https://orcid.org/0009-0008-6524-1231
Li, Niu https://orcid.org/0000-0001-6504-7633
Yang, Sijie https://orcid.org/0009-0007-5969-9775
Li, Youjin https://orcid.org/0000-0001-9898-6274
Zhou, Min https://orcid.org/0009-0006-7136-3070
Funding

Funding for this research was provided by:

National Natural Science Foundation of China (82071015)

Science and Technology Commission of Shanghai Municipality (21Y11900200)

Science and Technology Commission of Shanghai Municipality (22S31905600)
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Text and Data Mining valid from 2025-07-01

Text and Data Mining valid from 2025-07-01

Version of Record valid from 2025-03-10
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This article is maintained by: Elsevier

Article Title: Diagnosis of a patient with severe sensorineural hearing loss as the initial symptom caused by novel compound heterozygous variant in SLC19A2 gene

Journal Title: Brazilian Journal of Otorhinolaryngology

CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.bjorl.2025.101581

Content Type: article

Copyright: © 2025 Published by Elsevier España, S.L.U. on behalf of Associação Brasileira de Otorrinolaringologia e Cirurgia Cérvico-Facial.