Compound heterozygous mutations in WFS1 cause atypical Wolfram syndrome

Benzer Materyaller

• Familial Wolfram syndrome due to compound heterozygosity for two novel WFS1 mutations
  Yazar:: Zenteno, Juan Carlos, ve diğerleri
  Baskı/Yayın Bilgisi: (2008)
• Wolfram gene (WFS1) mutation causes autosomal dominant congenital nuclear cataract in humans
  Yazar:: Berry, Vanita, ve diğerleri
  Baskı/Yayın Bilgisi: (2013)
• Novel mutations in the WFS1 gene are associated with Wolfram syndrome and systemic inflammation
  Yazar:: Panfili, Eleonora, ve diğerleri
  Baskı/Yayın Bilgisi: (2021)
• Clinical Characteristics of Wolfram Syndrome in Chinese Population and a Novel Frameshift Mutation in WFS1
  Yazar:: Lian Duan, ve diğerleri
  Baskı/Yayın Bilgisi: (2018-02-01)
• Clinical Characteristics of Wolfram Syndrome in Chinese Population and a Novel Frameshift Mutation in WFS1
  Yazar:: Duan, Lian, ve diğerleri
  Baskı/Yayın Bilgisi: (2018)