Mutations at the SLC20A2 gene and brain resilience in families with idiopathic basal ganglia calcification (“Fahr's disease”)

Eitemau Tebyg

• Fahr disease: Idiopathic basal ganglia calcification
  gan: Shahidi, Gholam Ali, et al.
  Cyhoeddwyd: (2017)
• Familial idiopathic basal ganglia calcification (Fahr’s disease)
  gan: Mufaddel, Amir A., et al.
  Cyhoeddwyd: (2014)
• Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification
  gan: Hsu, Sandy Chan, et al.
  Cyhoeddwyd: (2013)
• Idiopathic Basal Ganglia Calcification: Fahr’s Syndrome, a Rare Disorder
  gan: Thillaigovindan, Ranjani, et al.
  Cyhoeddwyd: (2019)
• Loss of Function of Slc20a2 Associated with Familial Idiopathic Basal Ganglia Calcification in Humans Causes Brain Calcifications in Mice
  gan: Jensen, Nina, et al.
  Cyhoeddwyd: (2013)