Chinese Journal of Ophthalmology and Otorhinolaryngology, Volume. 25, Issue 4, 356(2025)
[in Chinese]
[1] [1] CUI T Y, GAO X, HUANG S S, et al. Four novel variants in POU4F3 cause autosomal dominant nonsyndromic hearing loss[J]. Neural Plast, 2020, 2020: 6137083. DOI: 10.1155/2020/6137083.
[2] [2] FU Y L, ZHA S W, L N Q, et al. Carrier frequencies of hearing loss variants in newborns of China: a meta-analysis[J]. J Evidence Based Medicine, 2019, 12(1): 40-50. DOI: 10.1111/jebm.12305.
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[in Chinese], [in Chinese], [in Chinese], [in Chinese], [in Chinese]. [J]. Chinese Journal of Ophthalmology and Otorhinolaryngology, 2025, 25(4): 356
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Received: Mar. 21, 2025
Accepted: Aug. 25, 2025
Published Online: Aug. 25, 2025
The Author Email: (yilai_shu@fudan.edu.cn)