A Novel SLC20A2 Mutation Associated with Familial Idiopathic Basal Ganglia Calcification and Analysis of the Genotype-Phenotype Association in Chinese Patients

Những quyển sách tương tự

• Association between a Novel Mutation in SLC20A2 and Familial Idiopathic Basal Ganglia Calcification
  Bằng: Zhang, Yang, et al.
  Được phát hành: (2013)
• Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification
  Bằng: Hsu, Sandy Chan, et al.
  Được phát hành: (2013)
• Mutations at the SLC20A2 gene and brain resilience in families with idiopathic basal ganglia calcification (“Fahr's disease”)
  Bằng: de Oliveira, Danyllo F., et al.
  Được phát hành: (2013)
• Mutation Analysis of SLC20A2 and SPP2 as Candidate Genes for Familial Idiopathic Basal Ganglia Calcification
  Bằng: Ashtari, Fereshteh, et al.
  Được phát hành: (2013)
• Loss of Function of Slc20a2 Associated with Familial Idiopathic Basal Ganglia Calcification in Humans Causes Brain Calcifications in Mice
  Bằng: Jensen, Nina, et al.
  Được phát hành: (2013)