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Paper Details

Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3p.
Blood
89
2010
197, 3p21, 9.4-Mb interval, AR-GPS gene, Chromosome 3p21, GPS, GPS gene, Gray platelet syndrome, causative gene, chromosome 3p, exons, gray platelets, hemorrhages, inherited bleeding disorder, myelofibrosis, myelofibrosis of GPS, patient, patients, platelet, platelet disorder, protein-coding genes, splenomegaly, thrombocytopenia, vitamin B(12)

Datasets

Release 1.2