Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome
Gray Platelet Syndrome (GPS) is a rare recessive bleeding disorder resulting from biallelic variants in NBEAL2. As part of a comprehensive evaluation of the phenotype and genotype in 47 patients with GPS, four different blood cell-types (platelets, neutrophils, monocytes, and CD4-lymphocytes) were evaluated using bulk RNA-seq in five patients and five controls. These data are deposited in this archive in FASTQ format.
- Type: Other
- 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 |
---|---|---|---|
EGAD00001005950 | Illumina HiSeq 4000 | 40 |
Publications | Citations |
---|---|
Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome.
Blood 136: 2020 1956-1967 |
23 |