Whole-exome study to identify the causative germline mutations of congenital macrothrombocytopenia
- Type: Exome Sequencing
- Archiver: European Genome-Phenome Archive (EGA)
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 | Illumina HiSeq 2000 | 21 |