Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes
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Published:2020-05-02
Issue:5
Volume:52
Page:473-481
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ISSN:1061-4036
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Container-title:Nature Genetics
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language:en
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Short-container-title:Nat Genet
Author:
Cortese AndreaORCID, Zhu Yi, Rebelo Adriana P.ORCID, 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., Rodriguez Aixa, Bacha Alexa, Kosikowski Ashley, Wood Beth, McCray Brett, Blume Brianna, Siskind Carly, Sumner Charlotte, Calabrese Daniela, Walk David, Vujovic Dragan, Park Eun, Muntoni Francesco, Donlevy Gabrielle, Acsadi Gyula, Day John, Burns Joshua, Li Jun, Krajewski Karen, Eichinger Kate, Cornett Kayla, Mullen Krista, Laura Perez Quiros, Gutmann Laurie, Barrett Maria, Saporta Mario, Skorupinska Mariola, Grant Natalie, Bray Paula, Seyedsadjadi Reza, Zuccarino Riccardo, Finkel Richard, Lewis Richard, Shy Rosemary R., Yum Sabrina, Hilbert Sarah, Thomas Simone, Behrens-Spraggins Steffen, Jones Tara, Lloyd Thomas, Grider Tiffany, Estilow Tim, Fridman Vera, 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. GraceORCID, Zuchner StephanORCID,
Publisher
Springer Science and Business Media LLC
Reference42 articles.
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