Charcot-Marie-Tooth disease: a novel Tyr145Ser mutation in the myelin protein zero (MPZ, P0) gene causes different phenotypes in homozygous and heterozygous carriers within one family

Παρόμοια τεκμήρια

• Pie cavo-varo en Charcot Marie Tooth
  ανά: Morales Llubere, Israel Eduardo
  Έκδοση: (2023)
• Immune effects of mesenchymal stem cells: Implications for Charcot–Marie–Tooth disease
  ανά: Leal Esquivel, Alejandro
  Έκδοση: (2008)
• Frecuency of the allele causing the axonal form of autosomal recessive Charcot-Marie-Tooth in Palmares, Costa Rica
  ανά: Rojas-Araya, Melissa
  Έκδοση: (2009)
• Distribución espacial de la enfermedad Charcot-Marie-Tooth en Costa Rica, 1990-2003
  ανά: Bonilla Carrión, Róger Enrique
  Έκδοση: (2009)
• Late onset autosomal dominant Charcot– Marie–Tooth 2 neuropathy in a Costa Rican family
  ανά: Berghoff, Corinna
  Έκδοση: (2009)