Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux (2017)
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/10.1038/s41598-017-15062-9
Publication URI: http://dx.doi.org/10.1038/s41598-017-15062-9
Type: Journal Article/Review
Parent Publication: Scientific Reports
Issue: 1