Clinical and Genetic Features in EYA1-Associated Branchio-Oto Syndrome: Cochlear Nerve Deficiency in Five of Thirteen Patients
- DOI
- 10.3390/diagnostics16152480
- Published
- 2026-08-06
- Container
- Diagnostics
- Publisher
- MDPI AG
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.3390/diagnostics16152480,
title = {Clinical and Genetic Features in EYA1-Associated Branchio-Oto Syndrome: Cochlear Nerve Deficiency in Five of Thirteen Patients},
author = {Yirong Niu and Yun Lin and Jiali Yu and Huanhuan Zhao and Yuting Zhao and Jie Chen and Ying Sun and Zeqi An and Mengping Wang and Kun Han and Hao Wu and Yun Li and Zhili Wang and Ying Chen},
year = {2026},
journal = {Diagnostics},
doi = {10.3390/diagnostics16152480},
url = {https://doi.org/10.3390/diagnostics16152480}
}RIS
TY - JOUR TI - Clinical and Genetic Features in EYA1-Associated Branchio-Oto Syndrome: Cochlear Nerve Deficiency in Five of Thirteen Patients AU - Yirong Niu AU - Yun Lin AU - Jiali Yu AU - Huanhuan Zhao AU - Yuting Zhao AU - Jie Chen AU - Ying Sun AU - Zeqi An AU - Mengping Wang AU - Kun Han AU - Hao Wu AU - Yun Li AU - Zhili Wang AU - Ying Chen PY - 2026 JO - Diagnostics DO - 10.3390/diagnostics16152480 UR - https://doi.org/10.3390/diagnostics16152480 ER -
APA
Niu, Y., Lin, Y., Yu, J., Zhao, H., Zhao, Y., Chen, J., Sun, Y., An, Z., Wang, M., Han, K., Wu, H., Li, Y., Wang, Z., & Chen, Y. (2026). Clinical and Genetic Features in EYA1-Associated Branchio-Oto Syndrome: Cochlear Nerve Deficiency in Five of Thirteen Patients. Diagnostics. https://doi.org/10.3390/diagnostics16152480
Source records
- crossref · retrieved 2026-09-26T12:52:14.355Z