A second locus for Schneckenbecken dysplasia identified by a mutation in the gene encoding inositol polyphosphate phosphatase-like 1 (INPPL1)

Am J Med Genet A. 2015 Oct;167A(10):2470-3. doi: 10.1002/ajmg.a.37173. Epub 2015 May 22.
No abstract available

Publication types

  • Case Reports
  • Research Support, N.I.H., Extramural

MeSH terms

  • Exome
  • Gene Expression
  • Genetic Loci*
  • Gestational Age
  • Homozygote
  • Humans
  • Hydrops Fetalis / genetics*
  • Hydrops Fetalis / pathology
  • Infant, Newborn
  • Male
  • Mutation*
  • Osteochondrodysplasias / genetics*
  • Osteochondrodysplasias / pathology
  • Phosphatidylinositol-3,4,5-Trisphosphate 5-Phosphatases
  • Phosphoric Monoester Hydrolases / genetics*
  • Stillbirth

Substances

  • Phosphoric Monoester Hydrolases
  • INPPL1 protein, human
  • Phosphatidylinositol-3,4,5-Trisphosphate 5-Phosphatases

Supplementary concepts

  • Schneckenbecken dysplasia