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Molecular analysis of a large novel deletion causing α(+)-thalassemia
BACKGROUND: α-thalassaemia is an inherited blood disorder caused by mutations in the α-globin gene cluster. Recognizing the pathogenic α-globin gene mutations associated with α-Thalassemia is of significant importance to thalassaemia’s diagnosis and management. METHODS: A family with α-thalassaemia...
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| Publicado no: | BMC Med Genet |
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| Main Authors: | , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6501318/ https://ncbi.nlm.nih.gov/pubmed/31060505 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-019-0797-8 |
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