Detection of 35delG, 167delT mutations in the connexin 26 gene among Egyptian patients with nonsyndromic sensorineural hearing loss
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Springer Science and Business Media LLC
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http://link.springer.com/content/pdf/10.4103/1012-5574.152707.pdf
Reference37 articles.
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1. Expanding the phenotypic spectrum in ESRRB related sensorineural hearing loss: Evidence provided via detecting novel nonsense mutation in an Egyptian family;Human Gene;2022-12
2. Genetic Screening for 35delG Mutation in Egyptian Patients with Profound Sensorineural Hearing Loss Scheduled for Cochlear Implantation: A Population-Based Study;ORL;2021
3. Breakdown of primary frequencies used in pediatric hearing screening with distortion-product otoacoustic emissions (DPOAEs);Hearing, Balance and Communication;2020-07-02
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