Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes (Nature Genetics, (2020), 52, 5, (473-481), 10.1038/s41588-020-0615-4)

Inherited Neuropathy Consortium

doi:10.1038/s41588-020-0649-7

Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes (Nature Genetics, (2020), 52, 5, (473-481), 10.1038/s41588-020-0615-4)

Inherited Neuropathy Consortium

Research output: Contribution to journal › Comment/debate › peer-review

Abstract

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Original language	English
Pages (from-to)	640
Number of pages	1
Journal	Nature Genetics
Volume	52
Issue number	6
DOIs	https://doi.org/10.1038/s41588-020-0649-7
Publication status	Published - Jun 1 2020

ASJC Scopus subject areas

Genetics

Access to Document

10.1038/s41588-020-0649-7

Fingerprint

Dive into the research topics of 'Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes (Nature Genetics, (2020), 52, 5, (473-481), 10.1038/s41588-020-0615-4)'. Together they form a unique fingerprint.

Cite this

Author Correction : Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes (Nature Genetics, (2020), 52, 5, (473-481), 10.1038/s41588-020-0615-4). / Inherited Neuropathy Consortium.

In: Nature Genetics, Vol. 52, No. 6, 01.06.2020, p. 640.

Research output: Contribution to journal › Comment/debate › peer-review

@article{442ca11a8b694c2cac9f0133496b94cf,

title = "Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes (Nature Genetics, (2020), 52, 5, (473-481), 10.1038/s41588-020-0615-4)",

abstract = "An amendment to this paper has been published and can be accessed via a link at the top of the paper.",

author = "{Inherited Neuropathy Consortium} and Andrea Cortese and Yi Zhu and Rebelo, {Adriana P.} and Sara Negri and Steve Courel and Lisa Abreu and Bacon, {Chelsea J.} and Yunhong Bai and Bis-Brewer, {Dana M.} and Enrico Bugiardini and Elena Buglo and Danzi, {Matt C.} and Feely, {Shawna M.E.} and Alkyoni Athanasiou-Fragkouli and Haridy, {Nourelhoda A.} and Aixa Rodriguez and Alexa Bacha and Ashley Kosikowski and Beth Wood and Brett McCray and Brianna Blume and Carly Siskind and Charlotte Sumner and Daniela Calabrese and David Walk and Dragan Vujovic and Eun Park and Francesco Muntoni and Gabrielle Donlevy and Gyula Acsadi and John Day and Joshua Burns and Jun Li and Karen Krajewski and Kate Eichinger and Kayla Cornett and Krista Mullen and Laura, {Perez Quiros} and Laurie Gutmann and Maria Barrett and Mario Saporta and Mariola Skorupinska and Natalie Grant and Stefania Magri and Chiara Pisciotta and Paola Saveri and Elena Grignani and Enrico Marchioni and Franco Taroni and Davide Pareyson",

year = "2020",

month = jun,

day = "1",

doi = "10.1038/s41588-020-0649-7",

language = "English",

volume = "52",

pages = "640",

journal = "Nature Genetics",

issn = "1061-4036",

publisher = "Nature Publishing Group",

number = "6",

}

TY - JOUR

T1 - Author Correction

T2 - Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes (Nature Genetics, (2020), 52, 5, (473-481), 10.1038/s41588-020-0615-4)

AU - Inherited Neuropathy Consortium

AU - Cortese, Andrea

AU - Zhu, Yi

AU - Rebelo, Adriana P.

AU - Negri, Sara

AU - Courel, Steve

AU - Abreu, Lisa

AU - Bacon, Chelsea J.

AU - Bai, Yunhong

AU - Bis-Brewer, Dana M.

AU - Bugiardini, Enrico

AU - Buglo, Elena

AU - Danzi, Matt C.

AU - Feely, Shawna M.E.

AU - Athanasiou-Fragkouli, Alkyoni

AU - Haridy, Nourelhoda A.

AU - Rodriguez, Aixa

AU - Bacha, Alexa

AU - Kosikowski, Ashley

AU - Wood, Beth

AU - McCray, Brett

AU - Blume, Brianna

AU - Siskind, Carly

AU - Sumner, Charlotte

AU - Calabrese, Daniela

AU - Walk, David

AU - Vujovic, Dragan

AU - Park, Eun

AU - Muntoni, Francesco

AU - Donlevy, Gabrielle

AU - Acsadi, Gyula

AU - Day, John

AU - Burns, Joshua

AU - Li, Jun

AU - Krajewski, Karen

AU - Eichinger, Kate

AU - Cornett, Kayla

AU - Mullen, Krista

AU - Laura, Perez Quiros

AU - Gutmann, Laurie

AU - Barrett, Maria

AU - Saporta, Mario

AU - Skorupinska, Mariola

AU - Grant, Natalie

AU - Magri, Stefania

AU - Pisciotta, Chiara

AU - Saveri, Paola

AU - Grignani, Elena

AU - Marchioni, Enrico

AU - Taroni, Franco

AU - Pareyson, Davide

PY - 2020/6/1

Y1 - 2020/6/1

N2 - An amendment to this paper has been published and can be accessed via a link at the top of the paper.

AB - An amendment to this paper has been published and can be accessed via a link at the top of the paper.

UR - http://www.scopus.com/inward/record.url?scp=85085979321&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85085979321&partnerID=8YFLogxK

U2 - 10.1038/s41588-020-0649-7

DO - 10.1038/s41588-020-0649-7

M3 - Comment/debate

C2 - 32457452

AN - SCOPUS:85085979321

SN - 1061-4036

VL - 52

SP - 640

JO - Nature Genetics

JF - Nature Genetics

IS - 6

ER -

Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes (Nature Genetics, (2020), 52, 5, (473-481), 10.1038/s41588-020-0615-4)

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this