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Homozygous missense WIPI2 variants cause a congenital disorder of autophagy with neurodevelopmental impairments of variable clinical severity and disease course. (2021)

First Author: Maroofian R

Attributed to: MRC Strategic Award to establish an International Centre for Genomic Medicine in Neuromuscular Diseases funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/braincomms/fcab183

PubMed Identifier: 34557665

Publication URI: http://europepmc.org/abstract/MED/34557665

Type: Journal Article/Review

Volume: 3

Parent Publication: Brain communications

Issue: 3

ISSN: 2632-1297