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Author Correction: Biallelic mutations in SORD cause a comm..:

Cortese, A ; Zhu, Y ; Rebelo, AP...
https://discovery.ucl.ac.uk/id/eprint/10100097/3/Reilly_Biallelic%20Expansion%20of%20an%20intronic%20Repeat%20in%20the%20RFC1%20Gene%20is%20a%20common%20cause%20of%20Late-Onset%20Ataxia%20manuscript_cortese_etal_22jan2019_accepted.pdf. , 2020

Link: https://discovery.ucl.ac.uk/id/eprint/10100097/3/Reill..

RT Journal
T1 <Title>Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftucl:oai:eprints.ucl.ac.uk.OAI2:10100097&Exemplar=1&LAN=DE
				
A1 Cortese, A
A1 Zhu, Y
A1 Rebelo, AP
A1 Negri, S
A1 Courel, S
A1 Abreu, L
A1 Bacon, CJ
A1 Bai, Y
A1 Bis-Brewer, DM
A1 Bugiardini, E
A1 Buglo, E
A1 Danzi, MC
A1 Feely, SME
A1 Athanasiou-Fragkouli, A
A1 Haridy, NA
A1 Inherited Neuropathy Consortium
A1 Isasi, R
A1 Khan, A
A1 Laurà, M
A1 Magri, S
A1 Pipis, M
A1 Pisciotta, C
A1 Powell, E
A1 Rossor, AM
A1 Saveri, P
A1 Sowden, JE
A1 Tozza, S
A1 Vandrovcova, J
A1 Dallman, J
A1 Grignani, E
A1 Marchioni, E
A1 Scherer, SS
A1 Tang, B
A1 Lin, Z
A1 Al-Ajmi, A
A1 Schüle, R
A1 Synofzik, M
A1 Maisonobe, T
A1 Stojkovic, T
A1 Auer-Grumbach, M
A1 Abdelhamed, MA
A1 Hamed, SA
A1 Zhang, R
A1 Manganelli, F
A1 Santoro, L
A1 Taroni, F
A1 Pareyson, D
A1 Houlden, H
A1 Herrmann, DN
A1 Reilly, MM
A1 Shy, ME
A1 Zhai, RG
A1 Zuchner, S
YR 2020
JF https://discovery.ucl.ac.uk/id/eprint/10100097/3/Reilly_Biallelic%20Expansion%20of%20an%20intronic%20Repeat%20in%20the%20RFC1%20Gene%20is%20a%20common%20cause%20of%20Late-Onset%20Ataxia%20manuscript_cortese_etal_22jan2019_accepted.pdf
LK http://dx.doi.org/https://discovery.ucl.ac.uk/id/eprint/10100097/3/Reilly_Biallelic%20Expansion%20of%20an%20intronic%20Repeat%20in%20the%20RFC1%20Gene%20is%20a%20common%20cause%20of%20Late-Onset%20Ataxia%20manuscript_cortese_etal_22jan2019_accepted.pdf
DO https://discovery.ucl.ac.uk/id/eprint/10100097/3/Reilly_Biallelic%20Expansion%20of%20an%20intronic%20Repeat%20in%20the%20RFC1%20Gene%20is%20a%20common%20cause%20of%20Late-Onset%20Ataxia%20manuscript_cortese_etal_22jan2019_accepted.pdf
SF ELIB - SuUB Bremen

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