par Reyniers, E;Van Bogaert, Patrick ;Peeters, N;Vits, L;Pauly, F;Fransen, E;Van Regemorter, Nicole ;Kooy, R F
Référence American journal of human genetics, 65, 5, page (1406-1412)
Publication Publié, 1999-11
Référence American journal of human genetics, 65, 5, page (1406-1412)
Publication Publié, 1999-11
Article révisé par les pairs
Résumé : | Choreoathetosis is a major clinical feature in only a small number of hereditary neurological disorders. We define a new X-linked syndrome with a unique clinical picture characterized by mild mental retardation, choreoathetosis, and abnormal behavior. We mapped the disease in a four-generation pedigree to chromosome Xp11 by linkage analysis and defined a candidate region containing a number of genes possibly involved in neuronal signaling, including a potassium channel gene and a neuronal G protein-coupled receptor. |