Stem Cell Research (Oct 2020)

Generation of two hiPSC clones (MHHi019-A, MHHi019-B) from a primary ciliary dyskinesia patient carrying a homozygous deletion in the NME5 gene (c.415delA (p.Ile139Tyrfs*8))

  • Anais Sahabian,
  • Laura von Schlehdorn,
  • Nora Drick,
  • Isabell Pink,
  • Julia Dahlmann,
  • Alexandra Haase,
  • Gudrun Göhring,
  • Tobias Welte,
  • Ulrich Martin,
  • Felix C. Ringshausen,
  • Ruth Olmer

Journal volume & issue
Vol. 48
p. 101988

Abstract

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Primary ciliary dyskinesia (PCD) is a genetic disorder characterized by defects in motile cilia and is known to occur in about 1 in 20,000 live births (Horani and Ferkol, 2018). Among the many genes associated with PCD, NME5, a gene encoding a protein involved in ciliary function, was recently reported to be involved in PCD (Anderegg et al., 2019; Cho et al., 2020). We have established two human induced pluripotent stem cell clones from a PCD patient carrying a deletion in the NME5 gene (c.415delA (p.Ile139Tyrfs*8)).