OBSL1 mutations in 3-M syndrome are associated with a modulation of IGFBP2 and IGFBP5 expression levels

Huber C., Fradin M., Edouard T., Le Merrer M., Alanay Y., Da Silva D. B., ...More

Human Mutation, vol.31, no.1, pp.20-26, 2010 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 31 Issue: 1
  • Publication Date: 2010
  • Doi Number: 10.1002/humu.21150
  • Journal Name: Human Mutation
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.20-26
  • Keywords: 3-M syndrome, OBSL1, growth retardation, IGFBP2, IGFBP5, GROWTH RETARDATION, MICE, FBXW8, CUL7
  • Acibadem Mehmet Ali Aydinlar University Affiliated: No