Gaparin, Maria Regina Franco Ribeiro; Crispim, Felipe; Paula, Sílvia; Freire, Maria Beatriz Sayeg; Dalbosco, Ivaldir Sabino; Della Manna, Thais; Salles, Joao Eduardo Nunes; Gasparin, Fábio; Guedes, Aléxis Dourado; Marcantonio, João; Gambine, Márcio; Salim, Camila Pitanga Calil; Moisés, Regina Célia Melo Santiago
(2009)
Objective: Wolfram syndrome (WS) is a rare, progressive, neurodegenerative disorder with an autosomal recessive pattern of inheritance. The gene for WS, WFS1, was identified on chromosome 4p16 and most WS patients carry ...
