Erratum to: PARP10 deficiency manifests by severe developmental delay and DNA repair defect (neurogenetics, (2016), 17, 4, (227-232), 10.1007/s10048-016-0493-1)

Maher Awni Shahrour; Claudia M. Nicolae; Simon Edvardson; Motee Ashhab; Adri M. Galvan; Daniel Constantin; Bassam Abu-Libdeh; George Lucian Moldovan; Orly Elpeleg

doi:10.1007/s10048-017-0511-y

Erratum to: PARP10 deficiency manifests by severe developmental delay and DNA repair defect (neurogenetics, (2016), 17, 4, (227-232), 10.1007/s10048-016-0493-1)

Maher Awni Shahrour
, Claudia M. Nicolae
, Simon Edvardson
, Motee Ashhab
, Adri M. Galvan
, Daniel Constantin
, Bassam Abu-Libdeh
, George Lucian Moldovan
, Orly Elpeleg

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

1 Scopus citations

Abstract

The original version of this article inadvertently contained a mistake. The Acknowledgment section of the paper states that the work was supported by the following grants: NIH 1R01ES026184, Department of Defense CA140303. However, NIH 1R01ES026184 and CA140303 funds were not used in the performance of this work. These grants were mistakenly included in the original paper.

Original language	English (US)
Pages (from-to)	119
Number of pages	1
Journal	Neurogenetics
Volume	18
Issue number	2
DOIs	https://doi.org/10.1007/s10048-017-0511-y
State	Published - Apr 1 2017

All Science Journal Classification (ASJC) codes

Genetics
Genetics(clinical)
Cellular and Molecular Neuroscience

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10.1007/s10048-017-0511-y

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Shahrour, M. A., Nicolae, C. M., Edvardson, S., Ashhab, M., Galvan, A. M., Constantin, D., Abu-Libdeh, B., Moldovan, G. L., & Elpeleg, O. (2017). Erratum to: PARP10 deficiency manifests by severe developmental delay and DNA repair defect (neurogenetics, (2016), 17, 4, (227-232), 10.1007/s10048-016-0493-1). Neurogenetics, 18(2), 119. https://doi.org/10.1007/s10048-017-0511-y

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abstract = "The original version of this article inadvertently contained a mistake. The Acknowledgment section of the paper states that the work was supported by the following grants: NIH 1R01ES026184, Department of Defense CA140303. However, NIH 1R01ES026184 and CA140303 funds were not used in the performance of this work. These grants were mistakenly included in the original paper.",

author = "Shahrour, \{Maher Awni\} and Nicolae, \{Claudia M.\} and Simon Edvardson and Motee Ashhab and Galvan, \{Adri M.\} and Daniel Constantin and Bassam Abu-Libdeh and Moldovan, \{George Lucian\} and Orly Elpeleg",

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doi = "10.1007/s10048-017-0511-y",

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Shahrour, MA, Nicolae, CM, Edvardson, S, Ashhab, M, Galvan, AM, Constantin, D, Abu-Libdeh, B, Moldovan, GL & Elpeleg, O 2017, 'Erratum to: PARP10 deficiency manifests by severe developmental delay and DNA repair defect (neurogenetics, (2016), 17, 4, (227-232), 10.1007/s10048-016-0493-1)', Neurogenetics, vol. 18, no. 2, pp. 119. https://doi.org/10.1007/s10048-017-0511-y

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AU - Shahrour, Maher Awni

AU - Nicolae, Claudia M.

AU - Edvardson, Simon

AU - Ashhab, Motee

AU - Galvan, Adri M.

AU - Constantin, Daniel

AU - Abu-Libdeh, Bassam

AU - Moldovan, George Lucian

AU - Elpeleg, Orly

PY - 2017/4/1

Y1 - 2017/4/1

N2 - The original version of this article inadvertently contained a mistake. The Acknowledgment section of the paper states that the work was supported by the following grants: NIH 1R01ES026184, Department of Defense CA140303. However, NIH 1R01ES026184 and CA140303 funds were not used in the performance of this work. These grants were mistakenly included in the original paper.

AB - The original version of this article inadvertently contained a mistake. The Acknowledgment section of the paper states that the work was supported by the following grants: NIH 1R01ES026184, Department of Defense CA140303. However, NIH 1R01ES026184 and CA140303 funds were not used in the performance of this work. These grants were mistakenly included in the original paper.

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DO - 10.1007/s10048-017-0511-y

M3 - Comment/debate

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SN - 1364-6745

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Erratum to: PARP10 deficiency manifests by severe developmental delay and DNA repair defect (neurogenetics, (2016), 17, 4, (227-232), 10.1007/s10048-016-0493-1)

Abstract

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