Genotype and Phenotype Spectrum of Charcot-Marie-Tooth Disease Due to Mutations in SORD.
Andrea Cortese, Maike F Dohrn, Riccardo Curro, Sara Negri, Petra Lassuthova,Chiara Pisciotta,Stefano Tozza, Abdullah Al-Ajmi, Changyoung Feng, Pedro J Tomaselli, Gorka Fernandez-Eulate, Saif Haddad,Matilde Laurà,Alexander M Rossor,Elisa Vegezzi, Stefano Facchini, James N Sleigh,Adriana Rebelo, Danique Beijer, Jacquelyn Raposo, Mario Saporta, Barbora Lauerova, Helena F Pernice, Pascal Achenbach, Ulrike Schöne, Tayir Alon, Marcus Deschauer, Isabell Cordts, Carolin D Obermaier, Natalie Winter, Peter D Creigh, Janet E Sowden, Tyler Rehbein, Stefania Magri,Alessandro Bertini,Paola Saveri,Paolo Ripellino, Jingyu Huang, Aleksandra Nadaj-Pakleza, Alison Ross, James K L Holt, Kathryn M Brennan, Rivka Sukenik-Halevy, Varoona Bizaoui, Yesim Parman, Esra Battaloglu,Arman Cakar, Hadil Alrohaif,Simon Hammans, Kishore R Kumar, Marina L Kennerson,Hülya Kayserili, Defne A Amado, Katrin Hahn,Paola Valentino, Francesca Cavalcanti, Carlo Gaetano,Franco Taroni, Geir J Braathen,Henry Houlden, Tanya Stojkovic, Stojan Peric,Alessandra Bolino, Stefano C Previtali, Yi-Chung Lee, Ayşe N Başak, Sherifa A Hamed, Ricardo Rojas-Garcia,Kristl G Claeys,Wilson Marques, Teresa Sevilla, Beate Schlotter-Weigel,Fiore Manganelli, Ruxu Zhang,David N Herrmann,Steven S Scherer,Pavel Seeman,Davide Pareyson,Mary M Reilly,Michael E Shy,Stephan Züchner
Brain a journal of neurology（2025）
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