Recurrent mutations in the NF1 gene are common among neurofibromatosis type 1 patients

مواد مشابهة

• A clinical variant of neurofibromatosis type 1: familial spinal neurofibromatosis with a frameshift mutation in the NF1 gene.
  بواسطة: Ars, E, وآخرون
  منشور في: (1998)
• Confirmation of a double-hit model for the NF1 gene in benign neurofibromas.
  بواسطة: Serra, E, وآخرون
  منشور في: (1997)
• Cold shock induces the insertion of a cryptic exon in the neurofibromatosis type 1 (NF1) mRNA
  بواسطة: Ars, Elisabet, وآخرون
  منشور في: (2000)
• Molecular characterization of the breakpoints of a 12-kb deletion in the NF1 gene in a family showing germ-line mosaicism.
  بواسطة: Lázaro, C, وآخرون
  منشور في: (1995)
• Independent NF1 mutations in two large families with spinal neurofibromatosis
  بواسطة: Messiaen, L, وآخرون
  منشور في: (2003)