ACTB Loss-of-Function Mutations Result in a Pleiotropic Developmental Disorder. (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/10.1016/j.ajhg.2017.11.006
PubMed Identifier: 29220674
Publication URI: http://europepmc.org/abstract/MED/29220674
Type: Journal Article/Review
Volume: 101
Parent Publication: American journal of human genetics
Issue: 6
ISSN: 0002-9297