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Globin gene transfer for treatment of the β-thalassemias and sickle cell disease

✍ Scribed by Michel Sadelain; Stefano Rivella; Leszek Lisowski; Selda Samakoglu; Isabelle Rivière

Book ID
119195220
Publisher
Elsevier Science
Year
2004
Tongue
English
Weight
212 KB
Volume
17
Category
Article
ISSN
1521-6926

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Sickle cell disorder, β-globin gene cluster haplotypes and α-thalassemia in neonates and adults from Guadeloupe
✍ Kéclard, L.; Romana, M.; Lavocat, E.; Saint-Martin, C.; Berchel, C.; Mérault, G. 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 47 KB 👁 1 views

We have studied haplotype of ␤ S chromosome and ␣-globin gene status in 534 patients (255 adults and 279 children of whom 159 neonates) from Guadeloupe with various sickle cell-related conditions, namely SS (n = 298), SC (n = 170), S-␤-thal (n = 56), and other rare forms (n = 10). Haplotype data on