Gene discovery for motile cilia disorders: mutation spectrum in primary ciliary dyskinesia and discovery of mutations in CCDC151

Ítems similars

• CCDC151 Mutations Cause Primary Ciliary Dyskinesia by Disruption of the Outer Dynein Arm Docking Complex Formation
  per: Hjeij, Rim, et al.
  Publicat: (2014)
• Phenotypic variability of CCDC103 mutation in British Pakistani children with Primary Ciliary Dyskinesia (PCD)
  per: Robson, E, et al.
  Publicat: (2015)
• Mutations in CCDC39 and CCDC40 are a major cause of primary ciliary dyskinesia with microtubule disorganisation
  per: Antony, D, et al.
  Publicat: (2012)
• Mutations in CCDC39 and CCDC40 are the major cause of primary ciliary dyskinesia with axonemal disorganisation and absent inner dynein arms
  per: Antony, Dinu, et al.
  Publicat: (2013)
• Immunofluorescence microscopy (IFM) analysis of primary ciliary dyskinesia (PCD) patients with suspected inner dynein arm defects (IDA)
  per: Hjeij, R, et al.
  Publicat: (2012)