Mutations in CCDC39 and CCDC40 are a major cause of primary ciliary dyskinesia with microtubule disorganisation

Παρόμοια τεκμήρια

• Mutations in CCDC39 and CCDC40 are the major cause of primary ciliary dyskinesia with axonemal disorganisation and absent inner dynein arms
  ανά: Antony, Dinu, κ.ά.
  Έκδοση: (2013)
• Phenotypic variability of CCDC103 mutation in British Pakistani children with Primary Ciliary Dyskinesia (PCD)
  ανά: Robson, E, κ.ά.
  Έκδοση: (2015)
• CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms
  ανά: Panizzi, Jennifer R., κ.ά.
  Έκδοση: (2012)
• Mutations in the dynein assembly factor PF22 (DNAAF3) cause primary ciliary dyskinesia with absent dynein arms
  ανά: Schmidts, M, κ.ά.
  Έκδοση: (2012)
• Gene discovery for motile cilia disorders: mutation spectrum in primary ciliary dyskinesia and discovery of mutations in CCDC151
  ανά: Onoufriadis, A, κ.ά.
  Έκδοση: (2015)