Medical genetics: advances in brief: Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene

Những quyển sách tương tự

• FATAL FAMILIAL INSOMNIA, A PRION DISEASE WITH A MUTATION AT CODON 178 OF THE PRION PROTEIN GENE
  Bằng: Medori, Rossella, et al.
  Được phát hành: (1992)
• Prion protein gene analysis in three kindreds with fatal familial insomnia (FFI): codon 178 mutation and codon 129 polymorphism.
  Bằng: Medori, R, et al.
  Được phát hành: (1993)
• Medical genetics: advances in brief: Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy
  Bằng: Norman, Andrew
  Được phát hành: (1992)
• Medical genetics: advances in brief
  Bằng: Norman, Andrew
  Được phát hành: (1992)
• Familial fatal insomnia with atypical clinical features in a patient with D178N mutation and homozygosity for Met at codon 129 of the prion protein gene
  Bằng: Sun, Lin, et al.
  Được phát hành: (2015)