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Clue to a New Deafness Gene: A Large Chinese Nonsyndromic Hearing Loss Family Linked to DFNA4

Liang Zong Chunye Lu Yali Zhao Qian Li Dongyi Han Weiyan Yang Yan Shen Qingyin Zheng Qiuju Wang

Liang Zong, Chunye Lu, Yali Zhao, Qian Li, Dongyi Han, Weiyan Yang, Yan Shen, Qingyin Zheng, Qiuju Wang. Clue to a New Deafness Gene: A Large Chinese Nonsyndromic Hearing Loss Family Linked to DFNA4[J]. Journal of Genetics and Genomics, 2012, 39(12): 653-657. doi: 10.1016/j.jgg.2012.11.002
Citation: Liang Zong, Chunye Lu, Yali Zhao, Qian Li, Dongyi Han, Weiyan Yang, Yan Shen, Qingyin Zheng, Qiuju Wang. Clue to a New Deafness Gene: A Large Chinese Nonsyndromic Hearing Loss Family Linked to DFNA4[J]. Journal of Genetics and Genomics, 2012, 39(12): 653-657. doi: 10.1016/j.jgg.2012.11.002

doi: 10.1016/j.jgg.2012.11.002

Clue to a New Deafness Gene: A Large Chinese Nonsyndromic Hearing Loss Family Linked to DFNA4

More Information
    Corresponding author: E-mail address: wqcr@263.net (Qiuju Wang)
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    [8] Goldstein, J.A., Lalwani, A.K. Further evidence for a third deafness gene within the DFNA2 locus Am. J. Med. Genet., 108 (2002),pp. 304-309
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    [13] Pusch, C.M., Meyer, B., Kupka, S. et al. Refinement of the DFNA4 locus to a 144 Mb region in 19q13.33 J. Mol. Med., 82 (2004),pp. 398-402
    [14] Ruel, J., Emery, S., Nouvian, R. et al. Impairment of SLC17A8 encoding vesicular glutamate transporter-3, VGLUT3, underlies nonsyndromic deafness DFNA25 and inner hair cell dysfunction in null mice Am. J. Hum. Genet., 83 (2008),pp. 278-292
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    [18] Xia, J.H., Liu, C.Y., Tang, B.S. et al. Mutations in the gene encoding gap junction protein β-3 associated with autosomal dominant hearing impairment Nat. Genet., 20 (1998),pp. 370-373
    [19] Yan, X.K., Zhang, T.Y., Wang, Z.M. et al. J. Genet. Genomics, 38 (2011),pp. 585-591
    [20] Yang, T., Pfister, M., Blin, N. et al. Genetic heterogeneity of deafness phenotypes linked to DFNA4 Am. J. Med. Genet., 139 (2005),pp. 9-12
    [21] Zhang, J., Chiodini, R., Badr, A. et al. The impact of next-generation sequencing on genomics J. Genet. Genomics, 38 (2011),pp. 95-109
    [22] Zheng, J., Miller, K.K., Yang, T. et al. Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with α-tectorin and is mutated in autosomal dominant hearing loss (DFNA4) Proc. Natl. Acad. Sci. USA, 108 (2011),pp. 4218-4223
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出版历程
  • 收稿日期:  2012-09-07
  • 录用日期:  2012-11-06
  • 修回日期:  2012-11-05
  • 网络出版日期:  2012-11-16
  • 刊出日期:  2012-12-20

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