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Genetic and phenotypic characterization of NKX6-2 -related spastic ataxia and hypomyelination (2019)

First Author: Chelban V

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/10.1111/ene.14082

PubMed Identifier: 31509304

Publication URI: http://europepmc.org/abstract/MED/31509304

Type: Journal Article/Review

Parent Publication: European Journal of Neurology

Issue: 2

ISSN: 1351-5101