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

First Author: William G. Newman

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/10.60692/r84h9-f7110

Publication URI: https://gresis.osc.int//doi/10.60692/r84h9-f7110

Type: Other