Associated Papers
Identification and phased de novo mutation of the EPS8L2 gene in a patient with progressive hearing loss: A case report.
Gan H et al.
Medicine, 2026
Expansion of Molecular and Clinical Aspects of EPS8L2 (DFNB106)-Associated Hearing Loss Emphasizes a Potential Therapeutic Window.
Owrang D et al.
Molecular Neurobiology, 2026
Molecular Analysis of Twelve Pakistani Families with Nonsyndromic or Syndromic Hearing Loss.
Wang R et al.
Genetic Testing and Molecular Biomarkers, 2017
[Genetic counseling and intervention for families with deaf-mute patients based on genetic testing: analysis of 5 families].
Dai P et al.
Zhonghua Yi Xue Za Zhi, 2007
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