Study
Whole-exome study to identify the causative germline mutations of congenital macrothrombocytopenia
| Study ID | Alternative Stable ID | Type |
|---|---|---|
| EGAS00001000371 | Exome Sequencing |
Study Description
NA
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 |
|---|---|---|---|
| EGAD00001000286 |
Whole-exome study of congenital macrothrombocytopenia
|
Illumina HiSeq 2000 | 21 |
Who archives the data?
