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A Large Panel of Isogenic APP and PSEN1 Mutant Human iPSC Neurons Reveals Shared Endosomal Abnormalities Mediated by APP β-CTFs, Not Aβ

12 Aug 2019

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 31416668
DOI: 10.1016/j.neuron.2019.07.010

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A Large Panel of Isogenic APP and PSEN1 Mutant Human iPSC Neurons Reveals Shared Endosomal Abnormalities Mediated by APP β-CTFs, Not AβPMID 31416668Read ↗

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