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Homozygous TAF1C variants are associated with a novel childhood-onset neurological phenotype. (2020)

First Author: Knuutinen O

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/10.1111/cge.13827

PubMed Identifier: 32779182

Publication URI: http://europepmc.org/abstract/MED/32779182

Type: Journal Article/Review

Volume: 98

Parent Publication: Clinical genetics

Issue: 5

ISSN: 0009-9163