A Truncating Mutation of CEP135 Causes Primary Microcephaly and Disturbed Centrosomal Function

Documenti analoghi

• A Truncating Mutation of CEP135 Causes Primary Microcephaly and Disturbed Centrosomal Function
  di: Hussain, Muhammad Sajid, et al.
  Pubblicazione: (2012)
• CDK6 associates with the centrosome during mitosis and is mutated in a large Pakistani family with primary microcephaly
  di: Muhammad Sajid Hussain, et al.
  Pubblicazione: (2013)
• An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan
  di: Rasool, Sajida, et al.
  Pubblicazione: (2020)
• CDK5RAP2 interaction with components of the Hippo signaling pathway may play a role in primary microcephaly
  di: Sukumaran, Salil K., et al.
  Pubblicazione: (2016)
• Abnormal centrosomal structure and duplication in Cep135-deficient vertebrate cells
  di: Inanç, Burcu, et al.
  Pubblicazione: (2013)