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Microglial phagolysosome dysfunction and altered neural communication amplify phenotypic severity in Prader-Willi Syndrome with larger deletion. (2024)

First Author: Correa-Da-Silva F

Attributed to: MRC Centre for Neuropsychiatric Genetics and Genomics funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1007/s00401-024-02714-0

PubMed Identifier: 38556574

Publication URI: http://europepmc.org/abstract/MED/38556574

Type: Journal Article/Review

Volume: 147

Parent Publication: Acta neuropathologica

Issue: 1

ISSN: 0001-6322