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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: Glenda M. Beaman

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/10.60692/9r4cj-aps36

Publication URI: https://gresis.osc.int//doi/10.60692/9r4cj-aps36

Type: Other