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Severe neurodevelopmental disease caused by a homozygous TLK2 variant. (2020)

First Author: Töpf A

Attributed to: Exosomal protein deficiencies: how abnormal RNA metabolism results in childhood-onset neurological diseases funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41431-019-0519-x

PubMed Identifier: 31558842

Publication URI: http://europepmc.org/abstract/MED/31558842

Type: Journal Article/Review

Volume: 28

Parent Publication: European journal of human genetics : EJHG

Issue: 3

ISSN: 1018-4813