Associated Papers
The Many Faces of DFNB9: Relating OTOF Variants to Hearing Impairment.
Vona B et al.
Genes, 2020
33256196 (PubMed )
Supplement: genes-11-01411-s001.xlsx › OTOF_NM_001287489
Identification of novel variants in MYO15A, OTOF, and RDX with hearing loss by next-generation sequencing.
Bai X et al.
Molecular Genetics & Genomic Medicine, 2019
[Mutational analysis of 117 patients with non-syndromic hearing loss].
Wang L et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2019
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