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Polymorphisms in Inflammatory Genes Modulate Clinical Complications in Patients With Sickle Cell Disease
Sickle cell disease (SCD), the most common monogenic disease worldwide, is marked by a phenotypic variability that is, to date, only partially understood. Because inflammation plays a major role in SCD pathophysiology, we hypothesized that single nucleotide polymorphisms (SNP) in genes encoding func...
Autores principales: | Tozatto-Maio, Karina, Girot, Robert, Ly, Indou Deme, Silva Pinto, Ana Cristina, Rocha, Vanderson, Fernandes, Francisco, Diagne, Ibrahima, Benzerara, Yahia, Dinardo, Carla L., Soler, Julia Pavan, Kashima, Simone, Araujo, Itauá Leston, Kenzey, Chantal, Fonseca, Guilherme H. H., Rodrigues, Evandra S., Volt, Fernanda, Jarduli, Luciana, Ruggeri, Annalisa, Mariaselvam, Christina, Gualandro, Sandra F. M., Rafii, Hanadi, Cappelli, Barbara, Nogueira, Felipe Melo, Scigliuolo, Graziana Maria, Guerino-Cunha, Renato Luiz, Malmegrim, Kelen Cristina Ribeiro, Simões, Belinda P., Gluckman, Eliane, Tamouza, Ryad |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7510050/ https://www.ncbi.nlm.nih.gov/pubmed/33013863 http://dx.doi.org/10.3389/fimmu.2020.02041 |
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