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Hydrocephalus

  • RESEARCH ARTICLE
    A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice
    Zakia Abdelhamed, Marshall Lukacs, Sandra Cindric, Saima Ali, Heymut Omran, Rolf W. Stottmann
    Disease Models & Mechanisms 2020 13: dmm045344 doi: 10.1242/dmm.045344 Published 30 October 2020

    Summary: The Spag17pcdo mouse model closely recapitulates the human central pair primary ciliary dyskinesia condition, and the data here reinforce the power of the hypomorphic allele in representing human conditions.

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