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Updated: May 19, 2026

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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Novel Frameshift Variant in SORL1 Gene Identified in a EOAD Family Causes APP Sorting Dysfunction and Endolysosomal

Gege Jiang1, Guanfeng Xie1, Liqin Huang1

  • 1Department of Neurology, Renmin Hospital of Wuhan University, Wuhan, 430060, Hubei Province, China.

Molecular Neurobiology
|May 18, 2026
PubMed
Abstract

Keywords:
SORL1Amyloid precursor proteinAmyloid-betaDementiaEndosome

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