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Genetic classification and confirmation of inherited platelet disorders: current status in Korea
Inherited platelet disorders (IPDs), which manifest as primary hemostasis defects, often underlie abnormal bleeding and a family history of thrombocytopenia, bone marrow failure, hematologic malignancies, undefined mucocutaneous bleeding disorder, or congenital bony defects. Wide heterogeneity in IP...
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| Publicat a: | Clin Exp Pediatr |
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| Autor principal: | |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Korean Pediatric Society
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7073384/ https://ncbi.nlm.nih.gov/pubmed/31477680 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3345/kjp.2019.00052 |
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