Sequence Variations and Haplotypes of the GJB2 Gene Revealed by Resequencing of 192 Chromosomes from the General Population in Korea
Hee-Jung Kim, Chang-Hun Park, Hee-Jin Kim, Ki-O Lee, Hong-Hee Won, Moon-Hee Ko, Hosuk Chu, Yang-Sun Cho, Won-Ho Chung, Jong-Won Kim, Sung Hwa Hong
Clin Exp Otorhinolaryngol. 2010;3(2):65-69.   Published online 2010 Jun 30     DOI: https://doi.org/10.3342/ceo.2010.3.2.65
Citations to this article as recorded by Crossref logo
The effectiveness of expanded carrier screening based on next-generation sequencing for severe monogenic genetic diseases
Xue Zhang, Qian Chen, Junnan Li, Xin Luo, Jianyun Luo, Jian Li, Ziye Zeng, Yan Wu, Hua Zhang, Yanling Dong
Human Genomics.2024;[Epub]     CrossRef
Machine learning-based genetic diagnosis models for hereditary hearing loss by the GJB2, SLC26A4 and MT-RNR1 variants
Xiaomei Luo, Fengmei Li, Wenchang Xu, Kaicheng Hong, Tao Yang, Jiansheng Chen, Xiaohe Chen, Hao Wu
eBioMedicine.2021; 69: 103322.     CrossRef
Evidence for Central Asian Origin of the p.Val27Ile Variant in the GJB2 Gene
Guille García Sánchez, Alfonso Alfaro-Rodríguez, Adrián Poblano
International Journal of Medical Genetics.2014; 2014: 1.     CrossRef
GJB2-associated hearing loss: Systematic review of worldwide prevalence, genotype, and auditory phenotype
Dylan K. Chan, Kay W. Chang
The Laryngoscope.2014; 124(2): E34.     CrossRef
Identification of a Novel Homozygous Mutation, TMPRSS3: c.535G>A, in a Tibetan Family with Autosomal Recessive Non-Syndromic Hearing Loss
Dongyan Fan, Wei Zhu, Dejun Li, De Ji, Ping Wang, Mathias Toft
PLoS ONE.2014; 9(12): e114136.     CrossRef
Etiology and Audiological Outcomes at 3 Years for 364 Children in Australia
Hans-Henrik M. Dahl, Teresa Y. C. Ching, Wendy Hutchison, Sanna Hou, Mark Seeto, Jessica Sjahalam-King, Andreas R. Janecke
PLoS ONE.2013; 8(3): e59624.     CrossRef