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

Documenti analoghi

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