An Amish founder variant consolidates disruption of CEP55 as a cause of hydranencephaly and renal dysplasia. (2019)
Attributed to:
Precision Medicine Exeter Innovation Platform (PMEI Platform): Proof of Concept Funds
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/s41431-018-0306-0
PubMed Identifier: 30622327
Publication URI: http://europepmc.org/abstract/MED/30622327
Type: Journal Article/Review
Volume: 27
Parent Publication: European journal of human genetics : EJHG
Issue: 4
ISSN: 1018-4813