Enlarged Vestibular Aqueduct Syndrome
What's New
Last Posted: Mar 06, 2023
- [Identification of a novel mutation of SLC26A4 gene with enlarged vestibular aqueduct syndrome].
Chen J, et al. Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery 2018 0 (9) 694-696 - [An analysis of the mutation in GJB2?GJB3?SLC26A4 and mtDNA12SrRNA in new born].
Chai F, et al. Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery 2017 5 (9) 664-666 - Application of a New Genetic Deafness Microarray for Detecting Mutations in the Deaf in China.
Wu Hong et al. PloS one 2016 11(3) e0151909 - Correlation analysis of genotypes, auditory function, and vestibular size in Chinese children with enlarged vestibular aqueduct syndrome.
Zhao Fei-Fan, et al. Acta oto-laryngologica 2013 12 (12) 1242-9 - [Diagnostic function of SLC26A4 hot spot mutations screening to enlarged vestibular aqueduct syndrome].
Li Qi, et al. Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery 2010 10 (19) 876-9 - Enlarged vestibular aqueduct syndrome
From NCATS Genetic and Rare Diseases Information Center - [Sequencing analysis of whole SLC26A4 gene related to IVS7-2A > G mutation in 1552 moderate to profound sensorineural hearing loss patients in China].
Yuan Yong-yi, et al. Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery 2009 6 (6) 449-54 - [Frequency of SLC26A4 IVS7-2A > G mutation in patients with severe to profound hearing loss from different area and ethnic group in China].
Li Qi, et al. Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery 2007 12 (12) 893-7 - [Sequencing of SLC26A4 exons 7 and 8 and hot spot mutation analysis in 1552 moderate to profound sensorineural hearing loss patients in China].
Dai Pu, et al. Zhonghua yi xue za zhi 2007 9 (36) 2521-5 - [The roles of connexin genes in sporadic hearing loss population].
Li Qing-zhong, et al. Zhonghua yi xue za zhi 2007 4 (16) 1097-101
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