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Detection of BCL11A and HBS1L-MYB Genotypes in Sickle Cell Anemia
Sickle Cell Anemia (SCA) is one of the most common monogenic disorders worldwide. Molecular modifiers of clinical symptoms play an essential role in the amelioration of the effects of the disease. Single Nucleotide Polymorphisms (SNPs) of the BCL11A gene and within the HBS1L-MYB intergenic region, w...
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| Publicado no: | Indian J Hematol Blood Transfus |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer India
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7573094/ https://ncbi.nlm.nih.gov/pubmed/33100714 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12288-020-01270-3 |
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