Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes.,Nature Genetics

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Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes.
Nature Genetics ( IF 30.8 ) Pub Date : 2020-05-26 , DOI: 10.1038/s41588-020-0649-7
Andrea Cortese _{1,

2,

3} , Yi Zhu _{4,

5} , Adriana P Rebelo ₁ , Sara Negri ₆ , Steve Courel ₁ , Lisa Abreu ₁ , Chelsea J Bacon ₇ , Yunhong Bai ₇ , Dana M Bis-Brewer ₁ , Enrico Bugiardini ₂ , Elena Buglo ₁ , Matt C Danzi ₁ , Shawna M E Feely ₇ , Alkyoni Athanasiou-Fragkouli ₂ , Nourelhoda A Haridy _{2,

8} , , Rosario Isasi ₁ , Alaa Khan _{2,

9} , Matilde Laurà ₂ , Stefania Magri ₁₀ , Menelaos Pipis ₂ , Chiara Pisciotta ₁₁ , Eric Powell ₁ , Alexander M Rossor ₂ , Paola Saveri ₁₁ , Janet E Sowden ₁₂ , Stefano Tozza ₁₃ , Jana Vandrovcova ₂ , Julia Dallman ₁₄ , Elena Grignani ₆ , Enrico Marchioni ₁₅ , Steven S Scherer ₁₆ , Beisha Tang ₁₇ , Zhiqiang Lin ₁₈ , Abdullah Al-Ajmi ₁₉ , Rebecca Schüle _{20,

21} , Matthis Synofzik _{20,

21} , Thierry Maisonobe ₂₂ , Tanya Stojkovic ₂₃ , Michaela Auer-Grumbach ₂₄ , Mohamed A Abdelhamed ₈ , Sherifa A Hamed ₈ , Ruxu Zhang ₁₈ , Fiore Manganelli ₁₃ , Lucio Santoro ₁₃ , Franco Taroni ₁₀ , Davide Pareyson ₁₁ , Henry Houlden ₂ , David N Herrmann ₁₂ , Mary M Reilly ₂ , Michael E Shy ₇ , R Grace Zhai _{4,

5} , Stephan Zuchner ₁

Affiliation

Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, USA.
Department of Neuromuscular Disease, UCL Queen Square Institute of Neurology and The National Hospital for Neurology, London, UK.
Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.
Department of Molecular and Cellular Pharmacology, University of Miami Miller School of Medicine, Miami, FL, USA.
Program in Molecular and Cellular Pharmacology, University of Miami Miller School of Medicine, Miami, FL, USA.
Istituiti Clinici Scientifici Maugeri IRCCS, Environmental Research Center, Pavia, Italy.
Department of Neurology, University of Iowa Carver College of Medicine, Iowa City, IA, USA.
Department of Neurology and Psychiatry, Faculty of Medicine, Assiut University Hospital, Assiut, Egypt.
Molecular Diagnostic Unit, Clinical Laboratory Department, King Abdullah Medical City in Makkah, Mecca, Saudi Arabia.
Unit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Unit of Rare Neurodegenerative and Neurometabolic Diseases, Department of Clinical Neurosciences, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Department of Neurology, University of Rochester, Rochester, NY, USA.
Department of Neuroscience, Reproductive Sciences and Odontostomatology, University of Naples "Federico II", Naples, Italy.
Department of Biology, University of Miami, Coral Gables, FL, USA.
IRCCS Mondino Foundation, Pavia, Italy.
Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Department of Neurology, Xiangya Hospital, Central South University, Changsha, China.
Department of Neurology, The Third Xiangya Hospital, Central South University, Changsha, China.
Division of Neurology, Department of Medicine, Al-Jahra Hospital, Al-Jahra, Kuwait.
Department of Neurodegenerative Disease, Hertie-Institute for Clinical Brain Research, and Center for Neurology, University of Tübingen, Tübingen, Germany.
German Center of Neurodegenerative Diseases (DZNE), Tübingen, Germany.
Department of Neurophysiology, AP-HP, Sorbonne Université, Hôpital Pitié Salpêtrière, Paris, France.
Centre de Référence des Maladies Neuromusculaires Nord/Est/Ile de France, AP-HP, Sorbonne Université, Hôpital Pitié-Salpêtrière, Paris, France.
Department of Orthopaedics and Traumatology, Medical University of Vienna, Vienna, Austria.