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Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals. (2023)

First Author: Saida K

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/10.1016/j.gim.2022.09.010

PubMed Identifier: 36318270

Publication URI: http://europepmc.org/abstract/MED/36318270

Type: Journal Article/Review

Volume: 25

Parent Publication: Genetics in medicine : official journal of the American College of Medical Genetics

Issue: 1

ISSN: 1098-3600