📣 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.

A recurrent de novo MAX p.Arg60Gln variant causes a syndromic overgrowth disorder through differential expression of c-Myc target genes. (2024)

First Author: Harris EL

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2023.11.010

PubMed Identifier: 38141607

Publication URI: http://europepmc.org/abstract/MED/38141607

Type: Journal Article/Review

Volume: 111

Parent Publication: American journal of human genetics

Issue: 1

ISSN: 0002-9297