MOLECULAR GENETIC CHARACTERIZATION OF
b-THALASSEMIA AND SICKLE CELL SYNDROME
IN THE ALBANIAN POPULATION
Babameto-Laku A1,*, Mitre A2, Berisha S2, Mokini V1, Roko D1
*Corresponding Author: Anila Babameto-Laku, University Hospital Center “Mother Teresa”, Faculty of Medicine,
Service of Medical Genetics, Rruga Dibres, 307, Tirana, Albania; Tel.: +68-20-94-170; Fax: +355-4-227-2782;
E-mail: laku62@yahoo.com
page: 45
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ACKNOWLEDGMENTS
We would like to gratefully acknowledge Dr.
Solange d’Angely, President of the Association “Cooperation
Educative et Medicale pour les Enfants
d’Albanie” (CEMPEA), Paris, France, for giving us the
opportunity of training at the Laboratory of Biochemistry
and Molecular Genetics, APHP, Creteil, Paris,
France, where the TTGE method was developed. We
are also grateful to Dr. Serge Pissard (Laboratory of
Biochemistry and Molecular Genetics, APHP, Creteil,
Paris, France) for his help.
Declaration of Interest: The authors report no
conflicts of interest. The authors alone are responsible
for the content and writing of this article. This manuscript
has not been published elsewhere and has not been
simultaneously submitted for publication elsewhere.
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