Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia

Lignende værker

• A pathogenic progranulin mutation and C9orf72 repeat expansion in a family with frontotemporal dementia
  af: Lashley, Tammaryn, et al.
  Udgivet: (2014)
• Pathological correlates of white matter hyperintensities in a case of progranulin mutation associated frontotemporal dementia
  af: Woollacott, Ione O.C., et al.
  Udgivet: (2018)
• Progranulin-associated primary progressive aphasia: A distinct phenotype?
  af: Rohrer, Jonathan D., et al.
  Udgivet: (2010)
• Parietal Lobe Deficits in Frontotemporal Lobar Degeneration Caused by a Mutation in the Progranulin Gene
  af: Rohrer, Jonathan D, et al.
  Udgivet: (2008)
• Neologistic jargon aphasia and agraphia in primary progressive aphasia
  af: Rohrer, Jonathan D., et al.
  Udgivet: (2009)