📣 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 homozygous missense variant in CHRM3 associated with familial urinary bladder disease (2019)

First Author: Beaman G

Attributed to: Molecular bases of congenital bladder disease: the urofacial syndome (UFS) funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1111/cge.13631

PubMed Identifier: 31441039

Publication URI: http://europepmc.org/abstract/MED/31441039

Type: Journal Article/Review

Parent Publication: Clinical Genetics

Issue: 6

ISSN: 0009-9163