A novel mutation in FRMD7 causing X-linked idiopathic congenital nystagmus in a large family

Gelijkaardige items

• Identification of Three Novel Mutations in the FRMD7 Gene for X-linked Idiopathic Congenital Nystagmus
  door: Zhang, Xiao, et al.
  Gepubliceerd in: (2014)
• A novel splicing mutation of the FRMD7 gene in a Chinese family with X-linked congenital nystagmus
  door: Hu, Ying, et al.
  Gepubliceerd in: (2012)
• Mutations in a novel member of the FERM family, FRMD7 cause X-linked idiopathic congenital nystagmus (NYS1)
  door: Tarpey, P, et al.
  Gepubliceerd in: (2006)
• A novel frame-shift mutation in FRMD7 causes X-linked idiopathic congenital nystagmus in a Chinese family
  door: Du, Wei, et al.
  Gepubliceerd in: (2011)
• A novel missense mutation in the FERM domain containing 7 (FRMD7) gene causing X-linked idiopathic congenital nystagmus in a Chinese family
  door: Liu, Zhirong, et al.
  Gepubliceerd in: (2013)