Chronic hemolytic anemia due to novel α-globin chain variants: critical location of the mutation within the gene sequence for a dominant effect

Por Préhu, Claude, Moradkhani, Kamran, Riou, Jean, Bahuau, Michel, Launay, Pierre, Martin, Natacha, Wajcman, Henri, Goossens, Michel, Galactéros, Frédéric
Publicado em 2009

Mutations in the paralogous human α-globin genes yielding identical hemoglobin variants

Por Moradkhani, Kamran, Préhu, Claude, Old, John, Henderson, Shirley, Balamitsa, Vera, Luo, Hong-Yuan, Poon, Man-Chiu, Chui, David H. K., Wajcman, Henri, Patrinos, George P.
Publicado em 2008

A Dominant Mutation in the Gene Encoding the Erythroid Transcription Factor KLF1 Causes a Congenital Dyserythropoietic Anemia

Por Arnaud, Lionel, Saison, Carole, Helias, Virginie, Lucien, Nicole, Steschenko, Dominique, Giarratana, Marie-Catherine, Prehu, Claude, Foliguet, Bernard, Montout, Lory, de Brevern, Alexandre G., Francina, Alain, Ripoche, Pierre, Fenneteau, Odile, Da Costa, Lydie, Peyrard, Thierry, Coghlan, Gail, Illum, Niels, Birgens, Henrik, Tamary, Hannah, Iolascon, Achille, Delaunay, Jean, Tchernia, Gil, Cartron, Jean-Pierre
Publicado em 2010