A novel splice mutation of HERG in a Chinese family with long QT syndrome

Gelijkaardige items

• A splice site mutation in hERG leads to cryptic splicing in human long QT syndrome
  door: Gong, Qiuming, et al.
  Gepubliceerd in: (2008)
• Multiple splicing defects caused by hERG splice site mutation 2592+1G>A associated with long QT syndrome
  door: Stump, Matthew R., et al.
  Gepubliceerd in: (2011)
• Identification of a novel mutation in a Chinese family with Nance-Horan syndrome by whole exome sequencing
  door: Hong, Nan, et al.
  Gepubliceerd in: (2014)
• A novel phenotype with splicing mutation identified in a Chinese family with desminopathy
  door: Fan, Peng, et al.
  Gepubliceerd in: (2019)
• Variable Expression of Long QT Syndrome Among Gene Carriers from Families with Five Different HERG Mutations
  door: Benhorin, Jesaia, et al.
  Gepubliceerd in: (2006)