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The transcription factor GATA1 regulates NBEAL2 expression through a long-distance enhancer
Gray platelet syndrome is named after the gray appearance of platelets due to the absence of α-granules. It is caused by recessive mutations in NBEAL2, resulting in macrothrombocytopenia and myelofibrosis. Though using the term gray platelets for GATA1 deficiency has been debated, a reduced number o...
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| Publicado no: | Haematologica |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Ferrata Storti Foundation
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5395110/ https://ncbi.nlm.nih.gov/pubmed/28082341 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2016.152777 |
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