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Advanced filters: Author: Xiayidan Alimu Clear advanced filters

  • Many sporadic cases of hypertrophic cardiomyopathy have unknown genetic basis. Here, the authors identify a mutation in the gene NAP1L1 to be associated with cases of hypertrophic cardiomyopathy, linking it to cGAS-STING-IFN signaling.

    • Cheng Lv
    • Xiayidan Alimu
    • Yibo Wang
    ResearchOpen Access
    Nature Communications
    Volume: 16, P: 1-17