A Mild Case of Jeune Syndrome Associated with a Recurrent Missense Variant in DYNC2H1: Confirmation of a Genotype-Phenotype Correlation

Klin Padiatr. 2024 Feb;236(2):145-147. doi: 10.1055/a-2235-6201. Epub 2024 Jan 15.
No abstract available

MeSH terms

  • Cytoplasmic Dyneins / genetics
  • Ellis-Van Creveld Syndrome* / genetics
  • Genetic Association Studies
  • Humans
  • Mutation
  • Mutation, Missense
  • Phenotype

Substances

  • DYNC2H1 protein, human
  • Cytoplasmic Dyneins

Supplementary concepts

  • Jeune syndrome