A dominant variant in the PDE1C gene is associated with nonsyndromic hearing loss Article

Wang, Li, Feng, Yong, Yan, Denise et al. (2018). A dominant variant in the PDE1C gene is associated with nonsyndromic hearing loss . 137(6-7), 437-446. 10.1007/s00439-018-1895-y

Open Access International Collaboration

cited authors

  • Wang, Li; Feng, Yong; Yan, Denise; Qin, Litao; Grati, M'hamed; Mittal, Rahul; Li, Tao; Sundhari, Abhiraami Kannan; Liu, Yalan; Chapagain, Prem; Blanton, Susan H; Liao, Shixiu; Liu, Xuezhong

sustainable development goals

authors

publication date

  • July 1, 2018

webpage

keywords

  • ADAPTATION
  • COMPONENTS
  • CYCLIC-AMP
  • ENDOLYMPHATIC SAC
  • EXPRESSION
  • Genetics & Heredity
  • HAIR-CELLS
  • INHIBITION
  • Life Sciences & Biomedicine
  • NITRIC-OXIDE SYNTHASE
  • PHOSPHODIESTERASE
  • SYSTEM
  • Science & Technology

Digital Object Identifier (DOI)

publisher

  • SPRINGER

start page

  • 437

end page

  • 446

volume

  • 137

issue

  • 6-7