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Lrig2 and Hpse2, mutated in urofacial syndrome, pattern nerves in the urinary bladder. (2019)

First Author: Roberts NA

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/10.1016/j.kint.2018.11.040

PubMed Identifier: 30885509

Publication URI: http://europepmc.org/abstract/MED/30885509

Type: Journal Article/Review

Volume: 95

Parent Publication: Kidney international

Issue: 5

ISSN: 0085-2538