Novel WDR35 mutations in patients with cranioectodermal dysplasia (Sensenbrenner syndrome)

Clin Genet. 2013 Jan;83(1):92-5. doi: 10.1111/j.1399-0004.2012.01880.x. Epub 2012 Apr 9.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Bone and Bones / abnormalities
  • Bone and Bones / physiopathology
  • Child
  • Craniosynostoses* / genetics
  • Craniosynostoses* / physiopathology
  • Cytoskeletal Proteins
  • Ectodermal Dysplasia* / genetics
  • Ectodermal Dysplasia* / physiopathology
  • Female
  • Hedgehog Proteins
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Mutation
  • Proteins / genetics*

Substances

  • Cytoskeletal Proteins
  • Hedgehog Proteins
  • Intracellular Signaling Peptides and Proteins
  • Proteins
  • WDR35 protein, human

Supplementary concepts

  • Cranioectodermal Dysplasia