Enabling Global Clinical Collaborations on Identifiable Patient Data: The Minerva Initiative. (2019)

First Author: Nellåker C
Attributed to:  Automated phenotyping to accurately infer functional variants in clinical genetics funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.3389/fgene.2019.00611

PubMed Identifier: 31417602

Publication URI: http://europepmc.org/abstract/MED/31417602

Type: Journal Article/Review

Volume: 10

Parent Publication: Frontiers in genetics

ISSN: 1664-8021