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Oxidative stress status, clinical outcome, and β-globin gene cluster haplotypes in pediatric patients with sickle cell disease

✍ Scribed by Iryna Rusanova; Germaine Escames; Gladys Cossio; Rosaura G. De Borace; Belgica Moreno; Mariam Chahboune; Luís C. López; Tomas Díez; Dario Acuña-Castroviejo

Book ID
114794851
Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
106 KB
Volume
85
Category
Article
ISSN
0902-4441

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✍ Arends, A.; Alvarez, M.; Velázquez, D.; Bravo, M.; Salazar, R.; Guevara, J.M.; C 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 32 KB 👁 1 views

Sickle cell anemia and ␣-thalassemia have a heterogeneous distribution in Venezuela with a high frequency in the coastal area (sea level) and few cases in the mountains. Most of our population is an ethnic admixture of Europeans (Spaniards colonists), Africans (slaves), and Amerindians. The purpose