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

First Author: Beaman GM

Attributed to: Investigating the emerging role of spliceosome mutations in craniofacial development disorders 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

Volume: 96

Parent Publication: Clinical genetics

Issue: 6

ISSN: 0009-9163