Amino acid 118 in the deafness causing (DFNA20/26) ACTG1 gene is a mutational hot spot Article

Wang, Li, Yan, Denise, Qin, Litao et al. (2018). Amino acid 118 in the deafness causing (DFNA20/26) ACTG1 gene is a mutational hot spot . 11 264-269. 10.1016/j.genrep.2018.04.011

cited authors

  • Wang, Li; Yan, Denise; Qin, Litao; Li, Tao; Liu, Hongjian; Li, Wan; Mittal, Rahul; Yong, Feng; Chapagain, Prem; Liao, Shixiu; Liu, Xuezhong

authors

publication date

  • June 1, 2018

webpage

keywords

  • ACTG1
  • ACTIN
  • DFNA20/26
  • FAMILY
  • FEATURES
  • Genetics & Heredity
  • HEARING IMPAIRMENT
  • Hearing loss
  • Heterogeneity
  • Life Sciences & Biomedicine
  • Next-generation sequencing
  • SPECTRUM
  • Science & Technology

Digital Object Identifier (DOI)

publisher

  • ELSEVIER

start page

  • 264

end page

  • 269

volume

  • 11