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pro vyhledávání: '"Amanda Bezerra de Sá, Araújo"'
Autor:
Betânia Lucena Domingues, Hatzlhofer, Diego Antonio, Pereira-Martins, Igor, de Farias Domingos, Gabriela da Silva, Arcanjo, Isabel, Weinhäuser, Diego Arruda, Falcão, Isabela Cristina Cordeiro, Farias, Jéssica Vitória Gadelha, de Freitas Batista, Luana Priscilla Laranjeira, Prado, Jéssica Maria Florencio, Oliveira, Thais Helena Chaves, Batista, Marcondes José de Vasconcelos Costa, Sobreira, Rodrigo Marcionilo, de Santana, Amanda Bezerra de Sá, Araújo, Manuela Albuquerque, de Melo, Bruna Vasconcelos, de Ancântara, Juan Luiz, Coelho-Silva, Ana Beatriz Lucas, de Moura Rafael, Danízia Menezes, de Lima Silva, Flávia Peixoto, Albuquerque, Magnun Nueldo Nunes, Santos, Ana Cláudia, Dos Anjos, Fernando Ferreira, Costa, Aderson, da Silva Araújo, Antonio Roberto, Lucena-Araújo, Marcos André Cavalcanti, Bezerra
Publikováno v:
Annals of hematology. 100(4)
Alpha thalassemia and beta-globin haplotype are considered classical genetic disease modifiers in sickle cell anemia (SCA) causing clinical heterogeneity. Nevertheless, their functional impact on SCA disease emergence and progression remains elusive.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::759b3a7c91ce543ea24d8fd00b2f2c08
https://pubmed.ncbi.nlm.nih.gov/33586016
https://pubmed.ncbi.nlm.nih.gov/33586016
