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Manifestations of HbSE sickle cell disease: a systematic review
BACKGROUND: Sickle cell disease (SCD) is commonly encountered in Africa and Middle Eastern countries. The causative mutation in the gene encoding the hemoglobin subunit β (HBB) leads to various genotypic variants of the disease. This results in varied phenotypes, with a spectrum of complications, fr...
Autores principales: | Khamees, Ibrahim, Ata, Fateen, Choudry, Hassan, Soliman, Ashraf T., De Sanctis, Vincenzo, Yassin, Mohamed A. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8207785/ https://www.ncbi.nlm.nih.gov/pubmed/34134694 http://dx.doi.org/10.1186/s12967-021-02931-1 |
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