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Lunapark deficiency leads to an autosomal recessive neurodevelopmental phenotype with a degenerative course, epilepsy and distinct brain anomalies. (2023)

First Author: Accogli A

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/10.1093/braincomms/fcad222

PubMed Identifier: 37794925

Publication URI: http://europepmc.org/abstract/MED/37794925

Type: Journal Article/Review

Volume: 5

Parent Publication: Brain communications

Issue: 5

ISSN: 2632-1297