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Homozygosity mapping with SNP arrays confirms 3p21 as a recessive locus for gray platelet syndrome and narrows the interval significantly
Gray platelet syndrome (GPS) is an inherited bleeding disorder characterized by thrombocytopenia and the absence of α-granules in platelets. Patients with GPS present with mild to moderate bleeding and many develop myelofibrosis. The genetic cause of GPS is unknown. We present 2 Native American fami...
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Main Authors: | , , , , , , , , , , |
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Format: | Artigo |
Language: | Inglês |
Published: |
American Society of Hematology
2011
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Subjects: | |
Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3069679/ https://ncbi.nlm.nih.gov/pubmed/21263149 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2010-12-322990 |
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