Novel deletion mutations of the PIH1D3 gene in an infertile young man with primary ciliary dyskinesia and his cousin with Kartagener's syndrome

Asian J Androl. 2021 May-Jun;23(3):330-332. doi: 10.4103/aja.aja_43_20.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Ciliary Motility Disorders / genetics*
  • Family Health
  • Humans
  • Intracellular Signaling Peptides and Proteins / analysis*
  • Intracellular Signaling Peptides and Proteins / genetics
  • Kartagener Syndrome / genetics*
  • Male
  • Sequence Deletion*

Substances

  • DNAAF6 protein, human
  • Intracellular Signaling Peptides and Proteins