识别SETBP1哈普洛缺陷分子通路,以使用诱导多能干细胞和神经疾病建模改进患者诊断

Nicole C Shaw1, Kevin Chen1, Kathryn O Farley1

  • 1The Kids Research Institute of Australia, The University of Western Australia, Nedlands, WA, Australia.

Molecular autism
|October 1, 2024
PubMed
概括

通过使用人类神经细胞来建模SETBP1哈普洛缺陷障碍 (SETBP1-HD). 遗传变异通过改变WNT和POL2RA途径引起了类似SETBP1-HD的表型,使GATA2与疾病扰乱有关.

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