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	61.	Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes. [electronic resource] by Cortese, Andrea Zhu, Yi Rebelo, Adriana P Negri, Sara Courel, Steve Abreu, Lisa Bacon, Chelsea J Bai, Yunhong Bis-Brewer, Dana M Bugiardini, Enrico Buglo, Elena Danzi, Matt C Feely, Shawna M E Athanasiou-Fragkouli, Alkyoni Haridy, Nourelhoda A Isasi, Rosario Khan, Alaa Laurà, Matilde Magri, Stefania Pipis, Menelaos Pisciotta, Chiara Powell, Eric Rossor, Alexander M Saveri, Paola Sowden, Janet E Tozza, Stefano Vandrovcova, Jana Dallman, Julia Grignani, Elena Marchioni, Enrico Scherer, Steven S Tang, Beisha Lin, Zhiqiang Al-Ajmi, Abdullah Schüle, Rebecca Synofzik, Matthis Maisonobe, Thierry Stojkovic, Tanya Auer-Grumbach, Michaela Abdelhamed, Mohamed A Hamed, Sherifa A Zhang, Ruxu Manganelli, Fiore Santoro, Lucio Taroni, Franco Pareyson, Davide Houlden, Henry Herrmann, David N Reilly, Mary M Shy, Michael E Zhai, R Grace Zuchner, Stephan Producer: 20200803 In: Nature genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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