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