Homozygous TAF1C variants are associated with a novel childhood-onset neurological phenotype (2020)
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
Parent Publication: Clinical Genetics
Issue: 5
ISSN: 0009-9163