Sickle cell disease: A distinction of two most frequent genotypes (HbSS and HbSC)

Sickle cell disease (SCD) consists of a group of hemoglobinopathies in which individuals present highly variable clinical manifestations. Sickle cell anemia (SCA) is the most severe form, while SC hemoglobinopathy (HbSC) is thought to be milder. Thus, we investigated the clinical manifestations and...

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Detaylı Bibliyografya
Yayımlandı:PLoS One
Asıl Yazarlar: da Guarda, Caroline Conceição, Yahouédéhou, Sètondji Cocou Modeste Alexandre, Santiago, Rayra Pereira, Neres, Joelma Santana dos Santos, Fernandes, Camila Felix de Lima, Aleluia, Milena Magalhães, Figueiredo, Camylla Vilas Boas, Fiuza, Luciana Magalhães, Carvalho, Suellen Pinheiro, de Oliveira, Rodrigo Mota, Fonseca, Cleverson Alves, Ndidi, Uche Samuel, Nascimento, Valma Maria Lopes, Rocha, Larissa Carneiro, Goncalves, Marilda Souza
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science 2020
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6988974/
https://ncbi.nlm.nih.gov/pubmed/31995624
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0228399
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