[NF1 mutation analysis in a Chinese family with neuro- fibromatosis type]

Yi Chuan. 2008 Mar;30(3):309-12. doi: 10.3724/sp.j.1005.2008.00309.
[Article in Chinese]

Abstract

A Chinese family affected with autosomal dominant disorder-neurofibromatosis type I was identified in this study. Linkage analysis was performed, and DNA sequencing for whole coding region of NF1 was carried out to identify the disease-causing mutation. The disease gene of the Chinese NF1 family was linked to NF1 locus, and a nonsense mutation, G1336X in the NF1 gene was identified. This mutation truncates the NF1 protein by 1 483 amino acid residues at the C-terminus, and is co-segregate with all the patients, but not present in unaffected individuals in the family. The present study demonstrated that G1336X mutation in the NF1 gene cause Neurofibromatosis type I in the family. To our knowledge, this mutation is firstly reported in Chinese population.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Asian People
  • Child
  • Codon, Nonsense / genetics*
  • Female
  • Genetic Linkage / genetics
  • Humans
  • Male
  • Neurofibromatosis 1 / genetics*
  • Neurofibromin 1 / genetics*
  • Pedigree
  • Polymerase Chain Reaction

Substances

  • Codon, Nonsense
  • Neurofibromin 1