Molecular basis of ciliary defects caused by compound heterozygous IFT144/WDR19 mutations found in cranioectodermal dysplasia

  • Ishida, Yamato
  • Kobayashi, Takuya
  • Chiba, Shuhei
  • Katoh, Yohei
  • Nakayama, Kazuhisa
Human Molecular Genetics 30(3-4):p 213-225, February 01, 2021. | DOI: 10.1093/hmg/ddab034
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