Whole-exome study to identify the causative germline mutations of congenital macrothrombocytopenia

Study ID Alternative Stable ID Type
EGAS00001000371 Exome Sequencing

Study Description


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
Whole-exome study of congenital macrothrombocytopenia
Illumina HiSeq 2000 21

Who archives the data?

There are no publications available