Study
Genetic factors underlying premature MI in Greek families without vessel disease
| Study ID | Alternative Stable ID | Type |
|---|---|---|
| EGAS00001000478 | Other |
Study Description
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
Study Datasets 1 dataset.
Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data
| Dataset ID | Description | Technology | Samples |
|---|---|---|---|
| EGAD00001002178 |
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
|
Illumina HiSeq 2000 | 8 |
Who archives the data?
