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pro vyhledávání: '"Carlos Isanta Otal"'
Autor:
Josep Oriol Casanovas Marsal, Elisa Viladés Palomar, Samira Bakali Badesa, Ana Gómez Martínez, Valle Recasens, María Ángeles Montañés Gracia, Sergio Felipe Pinzón Mariño, Ana María Villegas Martínez, Silvia Méndez Martínez, Paloma Ropero Gradilla, Francisco de Asís Bartol Puyal, Fernando Ataulfo González Fernández, Carlos Isanta Otal, Beatriz Cordón Ciordia, José Alejando García Ortego
Publikováno v:
Clinical Biochemistry. 94:80-82
Sickle cell disease (SCD) is a common hemoglobinopathy, secondary to alterations in the β globin chain, resulting in an abnormal hemoglobin variant named as hemoglobin S. These disorders show a wide phenotypical spectrum, and the prevalence of these
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b10a5122232ba487af5855d9b38ca679
https://doi.org/10.1016/j.clinbiochem.2021.04.016
https://doi.org/10.1016/j.clinbiochem.2021.04.016
