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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