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Biallelic NDUFA13 variants lead to a neurodevelopmental phenotype with gradual neurological impairment. (2025)

First Author: Kaiyrzhanov R

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/fcae453

PubMed Identifier: 39963288

Publication URI: http://europepmc.org/abstract/MED/39963288

Type: Journal Article/Review

Volume: 7

Parent Publication: Brain communications

Issue: 1

ISSN: 2632-1297