PGD in the lab for triplet repeat diseases — myotonic dystrophy, Huntington's disease and Fragile-X syndrome
Titel:
PGD in the lab for triplet repeat diseases — myotonic dystrophy, Huntington's disease and Fragile-X syndrome
Auteur:
Sermon, Karen Seneca, Sara De Rycke, Martine Goossens, Veerle Van de Velde, Hilde De Vos, Anick Platteau, Peter Lissens, Willy Van Steirteghem, André Liebaers, Inge