Investigation of the hearing levels of siblings affected by a single GJB2 variant: Possibility of genetic modifiers-Reference-Cited by-同舟云学术

Investigation of the hearing levels of siblings affected by a single GJB2 variant: Possibility of genetic modifiers

Published:2021-10 Issue: Volume:149 Page:110840
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Hosoya Makoto^ORCID,Fujioka Masato^ORCID,Nara Kiyomitsu^ORCID,Morimoto Noriko,Masuda Sawako^ORCID,Sugiuchi Tomoko,Katsunuma Sayaka,Takagi Akira^ORCID,Morita Noriko,Ogawa Kaoru,Kaga Kimitaka,Matsunaga Tatsuo^ORCID

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health

Reference26 articles.

1. Newborn hearing screening: the great omission;Mehl;Pediatrics,1998

2. The Colorado newborn hearing screening project, 1992-1999: on the threshold of effective population-based universal newborn hearing screening;Mehl;Pediatrics,2002

3. World Report on Hearing;WHO,2021

4. Genetic epidemiology of hearing impairment;Morton;Ann. N. Y. Acad. Sci.,1991

5. Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans;Zelante;Hum. Mol. Genet.,1997

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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. Genetic Factors Contribute to the Phenotypic Variability in GJB2-Related Hearing Impairment;The Journal of Molecular Diagnostics;2023-11