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Expanding the HPSE2 Genotypic Spectrum in Urofacial Syndrome, A Disease Featuring a Peripheral Neuropathy of the Urinary Bladder. (2022)

First Author: Beaman GM
Attributed to:  Preclinical gene therapy for genetic urinary bladder disease funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.3389/fgene.2022.896125

PubMed Identifier: 35812751

Publication URI: http://europepmc.org/abstract/MED/35812751

Type: Journal Article/Review

Volume: 13

Parent Publication: Frontiers in genetics

ISSN: 1664-8021