SORL1 deficiency in human excitatory neurons causes APP-dependent defects in the endolysosome-autophagy network
Author:
Publisher
Elsevier BV
Subject
General Biochemistry, Genetics and Molecular Biology
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2. The SORL1 p.Y1816C variant causes impaired endosomal dimerization and autosomal dominant Alzheimer’s disease;Proceedings of the National Academy of Sciences;2024-09-03
3. Accumulation of APP C-terminal fragments causes endolysosomal dysfunction through the dysregulation of late endosome to lysosome-ER contact sites;Developmental Cell;2024-06
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