A novel missense mutation of the EDA gene in a Mongolian family with congenital hypodontia

This publication has 6 references indexed in Scilit:

• Edar/Eda interactions regulate enamel knot formation in tooth morphogenesis
  Development, 2000
• Ectodysplasin is a collagenous trimeric type II membrane protein with a tumor necrosis factor-like domain and co-localizes with cytoskeletal structures at lateral and apical surfaces of cells.
  Human Molecular Genetics, 1999
• The Anhidrotic Ectodermal Dysplasia Gene (EDA) Undergoes Alternative Splicing and Encodes Ectodysplasin-A with Deletion Mutations in Collagenous Repeats
  Human Molecular Genetics, 1998
• Identification of a New Splice Form of the EDA1 Gene Permits Detection of Nearly All X-Linked Hypohidrotic Ectodermal Dysplasia Mutations
  American Journal of Human Genetics, 1998
• X–linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein
  Nature Genetics, 1996
• Ectodermal dysplasias: A clinical classification and a causal review
  American Journal of Medical Genetics, 1994