ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss Article

Li, Wu, Sun, Jie, Ling, Jie et al. (2018). ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss . 137(4), 329-342. 10.1007/s00439-018-1885-0

International Collaboration

cited authors

  • Li, Wu; Sun, Jie; Ling, Jie; Li, Jiada; He, Chufeng; Liu, Yalan; Chen, Hongsheng; Men, Meichao; Niu, Zhijie; Deng, Yuyuan; Li, Meng; Li, Taoxi; Wen, Jie; Sang, Shushan; Li, Haibo; Wan, Zhengqing; Richard, Elodie M; Chapagain, Prem; Yan, Denise; Liu, Xue Zhong; Mei, Lingyun; Feng, Yong

publication date

  • April 1, 2018

keywords

  • C-ELEGANS
  • CELL-MIGRATION
  • CHINESE FAMILY
  • CRKII/DOCK180/RAC PATHWAY
  • DEAFNESS
  • EVOLUTIONARY
  • GJB2
  • GTPASE-ACTIVATING PROTEIN
  • Genetics & Heredity
  • IMPAIRMENT
  • Life Sciences & Biomedicine
  • MUTATIONS
  • Science & Technology

Digital Object Identifier (DOI)

start page

  • 329

end page

  • 342

volume

  • 137

issue

  • 4