📣 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.

Mutations in thyroid hormone receptor a1 cause premature neurogenesis and progenitor cell depletion in human cortical development. (2019)

First Author: Krieger TG

Attributed to: Wellcome Trust MRC Cambridge Stem Cell Institute funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1073/pnas.1908762116

PubMed Identifier: 31628250

Publication URI: http://europepmc.org/abstract/MED/31628250

Type: Journal Article/Review

Volume: 116

Parent Publication: Proceedings of the National Academy of Sciences of the United States of America

Issue: 45

ISSN: 0027-8424