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Publication Detail
Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes.
  • Publication Type:
    Journal article
  • Publication Sub Type:
    Corrigendum
  • Authors:
    Cortese A, Zhu Y, Rebelo AP, Negri S, Courel S, Abreu L, Bacon CJ, Bai Y, Bis-Brewer DM, Bugiardini E, Buglo E, Danzi MC, Feely SME, Athanasiou-Fragkouli A, Haridy NA, Inherited Neuropathy Consortium , Isasi R, Khan A, Laurà M, Magri S, Pipis M, Pisciotta C, Powell E, Rossor AM, Saveri P, Sowden JE, Tozza S, Vandrovcova J, Dallman J, Grignani E, Marchioni E, Scherer SS, Tang B, Lin Z, Al-Ajmi A, Schüle R, Synofzik M, Maisonobe T, Stojkovic T, Auer-Grumbach M, Abdelhamed MA, Hamed SA, Zhang R, Manganelli F, Santoro L, Taroni F, Pareyson D, Houlden H, Herrmann DN, Reilly MM, Shy ME, Zhai RG, Zuchner S
  • Publication date:
    26/05/2020
  • Journal:
    Nat Genet
  • Status:
    Published
  • Country:
    United States
  • PII:
    10.1038/s41588-020-0649-7
  • Language:
    eng
Abstract
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
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Department of Neuromuscular Diseases
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Department of Neuromuscular Diseases
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Department of Neuromuscular Diseases
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Developmental Neurosciences Dept
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Department of Neuromuscular Diseases
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Department of Neuromuscular Diseases
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