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Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus. (2014)

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/10.1093/hmg/ddu147

PubMed Identifier: 24691552

Publication URI: http://europepmc.org/abstract/MED/24691552

Type: Journal Article/Review

Volume: 23

Parent Publication: Human molecular genetics

Issue: 16

ISSN: 0964-6906