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Allelic and phenotypic heterogeneity in Junctophillin-3 related neurodevelopmental and movement disorders (2021)

First Author: Bourinaris T

Attributed to: Leveraging the power of genomics and transcriptomics to revolutionise the diagnosis and understanding of neurological disorders funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41431-021-00866-1

PubMed Identifier: 33824468

Publication URI: http://europepmc.org/abstract/MED/33824468

Type: Journal Article/Review

Parent Publication: European Journal of Human Genetics

Issue: 6

ISSN: 1018-4813