A homozygous missense variant in CHRM3 associated with familial urinary bladder disease. (2019)
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
Volume: 96
Parent Publication: Clinical genetics
Issue: 6
ISSN: 0009-9163