Late postnatal onset of hearing loss due to GJB2 mutations
Author:
Publisher
Elsevier BV
Subject
Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health
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4. Connexin-26 mutations in sporadic and inherited sensorineural deafness;Estivill;Lancet,1998
5. High carrier frequency of the 35delG deafness mutation in European populations. Genetic Analysis Consortium of GJB2 35delG;Gasparini;Eur. J. Hum. Genet.,2000
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1. Hearing and Hearing Loss Progression in Patients with GJB2 Gene Mutations: A Long-Term Follow-Up;International Journal of Molecular Sciences;2023-11-25
2. Audiological Evidence of Frequent Hereditary Mild, Moderate and Moderate-to-Severe Hearing Loss;Journal of Personalized Medicine;2022-11-04
3. Phenotypic Heterogeneity of Post-lingual and/or Milder Hearing Loss for the Patients With the GJB2 c.235delC Homozygous Mutation;Frontiers in Cell and Developmental Biology;2021-02-26
4. Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China;The American Journal of Human Genetics;2019-10
5. Prevalence and audiological profiles of GJB2 mutations in a large collective of hearing impaired patients;Hearing Research;2016-03
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