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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:PLoS One
Hauptverfasser: 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
Format: Artigo
Sprache:Inglês
Veröffentlicht: Public Library of Science 2020
Schlagworte:
Research Article
Online Zugang: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
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!

Ähnliche Einträge