EGAS00001000478-sc-20160608 - samples
Ontology highlight
ABSTRACT: The study will analyse by exome sequencing 8 Greek family members with an excess of potentially damaging mutations relating to premature MI and no vessel disease, to identify genetic factors underlying this condition. This is a follow on from project GPMI-NVD
PROVIDER: EGAD00001002178 | EGA |
REPOSITORIES: EGA
ACCESS DATA