📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome. (2019)

First Author: Vetrini F

Attributed to: The Northern Ireland Genomic Medicine Centre funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1186/s13073-019-0630-1

PubMed Identifier: 30909959

Publication URI: http://europepmc.org/abstract/MED/30909959

Type: Journal Article/Review

Volume: 11

Parent Publication: Genome medicine

Issue: 1

ISSN: 1756-994X