Familial STAG2 germline mutation defines a new human cohesinopathy. (2017)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41525-017-0009-4

PubMed Identifier: 29263825

Publication URI: http://europepmc.org/abstract/MED/29263825

Type: Journal Article/Review

Volume: 2

Parent Publication: NPJ genomic medicine

ISSN: 2056-7944