Charcot-Marie-Tooth families in Japan with MPZ Thr124Met mutation

Benzer Materyaller

• Charcot-Marie-Tooth families in Japan with MPZ Thr124Met mutation
  Yazar:: Kurihara, S, ve diğerleri
  Baskı/Yayın Bilgisi: (2004)
• An axonal form of Charcot-Marie-Tooth disease showing distinctive features in association with mutations in the peripheral myelin protein zero gene (Thr124Met or Asp75Val)
  Yazar:: Misu, K, ve diğerleri
  Baskı/Yayın Bilgisi: (2000)
• A Costa Rican family affected with Charcot-Marie-Tooth disease due to the myelin protein zero (MPZ) p.Thr124Met mutation shares the Belgian haplotype
  Yazar:: Alejandro Leal, ve diğerleri
  Baskı/Yayın Bilgisi: (2014)
• Histopathology of the inner ear in Charcot-Marie-Tooth Syndrome caused by a missense variant (p.Thr65Ala) in the MPZ gene
  Yazar:: Nadol, Joseph B., ve diğerleri
  Baskı/Yayın Bilgisi: (2019)
• CHARCOT-MARIE-TOOTH DISEASE
  Yazar:: Lea Leonardis, ve diğerleri
  Baskı/Yayın Bilgisi: (2003-09-01)