Erratum: Hwang Y.T. et al. Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia. Genes 2016, 7, 68
by
,
Yun Tae Hwang
1,2, 
Tracy Dudding
3,4,
Solange Mabel Aliaga
5,6,7,
Marta Arpone
5,6,10,
David Francis
5,
Xin Li
5,
Howard Robert Slater
5,6,
Carolyn Rogers
3,
Lesley Bretherton
8,9,10,
Desirée Du Sart
11,
Robert Heard
12,13,† and
David Eugeny Godler
5,*,† 1
Department of Neurology, Gosford Hospital, Gosford 2250, Australia
2
Institute of Neurology, University College London, London WC1N 3BG, UK
3
Genetics of Learning Disability Service, Hunter Genetics, Waratah 2298, Australia
4
Grow Up Well Priority Research Centre, University of Newcastle, Waratah 2308, Australia
5
Cyto-molecular Diagnostic Research Laboratory, Victorian Clinical Genetics Services and Murdoch Childrens Research Institute, Royal Children’s Hospital, Melbourne 3052, Australia
6
Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Melbourne 3010, Australia
7
Molecular and Cytogenetics Laboratory, INTA University of Chile, Santiago 7830490, Chile
8
Psychology Service, Royal Children’s Hospital, Melbourne 3052, Australia
9
Melbourne School of Psychological Sciences, University of Melbourne, Melbourne 3052, Australia
10
Child Neuropsychology, Murdoch Childrens Research Institute, Royal Children’s Hospital, Melbourne 3052, Australia
11
Molecular Genetics Laboratory, Victorian Clinical Genetics Services and Murdoch Childrens Research Institute, Royal Children’s Hospital, Melbourne 3052, Australia
12
Faculty of Medicine, University of Newcastle, Newcastle 2303, Australia
13
Westmead Millennium Institute, University of Sydney, Westmead 2145, Australia
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Genes 2017, 8(2), 47; https://doi.org/10.3390/genes8020047
Submission received: 20 January 2017
/
Revised: 20 January 2017
/
Accepted: 20 January 2017
/
Published: 24 January 2017
(This article belongs to the Section Human Genomics and Genetic Diseases)
The authors wish to make the following correction to their paper [1]. The authors’ affiliations are wrong and should be replaced with:
Yun Tae Hwang 1,2, Tracy Dudding 3,4, Solange Mabel Aliaga 5,6,7, Marta Arpone 5,6,10, David Francis 5, Xin Li 5, Howard Robert Slater 5,6, Carolyn Rogers 3, Lesley Bretherton 8,9,10, Desirée du Sart 11, Robert Heard 12,13,† and David Eugeny Godler 5,*,†
- 1
- Department of Neurology, Gosford Hospital, Gosford 2250, Australia; [email protected]
- 2
- Institute of Neurology, University College London, London WC1N 3BG, UK
- 3
- Genetics of Learning Disability Service, Hunter Genetics, Waratah 2298, Australia; [email protected] (T.D.); [email protected] (C.R.)
- 4
- Grow Up Well Priority Research Centre, University of Newcastle, Waratah 2308, Australia
- 5
- Cyto-molecular Diagnostic Research Laboratory, Victorian Clinical Genetics Services and Murdoch Childrens Research Institute, Royal Children’s Hospital, Melbourne 3052, Australia; [email protected] (S.M.A.); [email protected] (M.A.); [email protected] (D.F.); [email protected] (X.L.); [email protected] (H.R.S.)
- 6
- Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Melbourne 3010, Australia
- 7
- Molecular and Cytogenetics Laboratory, INTA University of Chile, Santiago 7830490, Chile
- 8
- Psychology Service, Royal Children’s Hospital, Melbourne 3052, Australia; [email protected]
- 9
- Melbourne School of Psychological Sciences, University of Melbourne, Melbourne 3052 Australia
- 10
- Child Neuropsychology, Murdoch Childrens Research Institute, Royal Children’s Hospital, Melbourne 3052, Australia
- 11
- Molecular Genetics Laboratory, Victorian Clinical Genetics Services and Murdoch Childrens Research Institute, Royal Children’s Hospital, Melbourne 3052, Australia; [email protected]
- 12
- Faculty of Medicine, University of Newcastle, Newcastle 2303, Australia; [email protected]
- 13
- Westmead Millennium Institute, University of Sydney, Westmead 2145, Australia
- *
- Correspondence: [email protected]; Tel.: +61-3-8341-6496; Fax: +61-3-9348-1391
- †
- These authors contributed equally to this work.
The authors would like to apologize for any inconvenience caused. The change does not affect the scientific results. The manuscript will be updated and the original will remain online on the article webpage.
Conflicts of Interest
The authors declare no conflict of interest.
Reference
- Hwang, Y.T.; Dudding, T.; Aliaga, S.M.; Arpone, M.; Francis, D.; Li, X.; Slater, H.R.; Rogers, C.; Bretherton, L.; du Sart, D.; et al. Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia. Genes 2016, 7, 68. [Google Scholar] [CrossRef] [PubMed]
© 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).
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MDPI and ACS Style
Hwang, Y.T.; Dudding, T.; Aliaga, S.M.; Arpone, M.; Francis, D.; Li, X.; Slater, H.R.; Rogers, C.; Bretherton, L.; Du Sart, D.; et al. Erratum: Hwang Y.T. et al. Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia. Genes 2016, 7, 68. Genes 2017, 8, 47. https://doi.org/10.3390/genes8020047
AMA Style
Hwang YT, Dudding T, Aliaga SM, Arpone M, Francis D, Li X, Slater HR, Rogers C, Bretherton L, Du Sart D, et al. Erratum: Hwang Y.T. et al. Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia. Genes 2016, 7, 68. Genes. 2017; 8(2):47. https://doi.org/10.3390/genes8020047
Chicago/Turabian StyleHwang, Yun Tae, Tracy Dudding, Solange Mabel Aliaga, Marta Arpone, David Francis, Xin Li, Howard Robert Slater, Carolyn Rogers, Lesley Bretherton, Desirée Du Sart, and et al. 2017. "Erratum: Hwang Y.T. et al. Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia. Genes 2016, 7, 68" Genes 8, no. 2: 47. https://doi.org/10.3390/genes8020047
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