📣 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.

PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature. (2018)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1136/jmedgenet-2017-104946

PubMed Identifier: 29097605

Publication URI: http://europepmc.org/abstract/MED/29097605

Type: Journal Article/Review

Volume: 55

Parent Publication: Journal of medical genetics

Issue: 2

ISSN: 0022-2593