Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes (vol 16, pg 613, 2020)
Andrea Cortese,Yi Zhu,Adriana P. Rebelo,Sara Negri,Steve Courel,Lisa Abreu,Chelsea J. Bacon,Yunhong Bai,Dana M. Bis-Brewer,Enrico Bugiardini,Elena Buglo,Matt C. Danzi,Shawna M. E. Feely,Alkyoni Athanasiou-Fragkouli,Nourelhoda A. Haridy,Rosario Isasi,Alaa Khan,Matilde Laura,Stefania Magri,Menelaos Pipis,Chiara Pisciotta,Eric Powell,Alexander M. Rossor,Paola Saveri,Janet E. Sowden,Stefano Tozza,Jana Vandrovcova,Julia Dallman,Elena Grignani,Enrico Marchioni,Steven S. Scherer,Beisha Tang,Zhiqiang Lin,Abdullah Al-Ajmi,Rebecca Schule,Matthis Synofzik,Thierry Maisonobe,Tanya Stojkovic,Michaela Auer-Grumbach, Mohamed A. Abdelhamed,Sherifa A. Hamed,Ruxu Zhang,Fiore Manganelli,Lucio Santoro,Franco Taroni,Davide Pareyson,Henry Houlden,David N. Herrmann,Mary M. Reilly,Michael E. Shy,R. Grace Zhai,Stephan Zuchner NATURE GENETICS（2020）
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