Erratum to: PARP10 deficiency manifests by severe developmental delay and DNA repair defect (Neurogenetics, (2016), 17, (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/s10048-016-0503-3

Erratum to: PARP10 deficiency manifests by severe developmental delay and DNA repair defect (Neurogenetics, (2016), 17, (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 authors, editors and publisher confirmthat patient consent to publish the patient’s photographs was obtained. This information was mistakenly omitted in the original paper.

Original language	English (US)
Pages (from-to)	71
Number of pages	1
Journal	Neurogenetics
Volume	18
Issue number	1
DOIs	https://doi.org/10.1007/s10048-016-0503-3
State	Published - Jan 1 2017

All Science Journal Classification (ASJC) codes

Genetics
Genetics(clinical)
Cellular and Molecular Neuroscience

Access to Document

10.1007/s10048-016-0503-3

Cite this

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, (227-232), 10.1007/s10048-016-0493-1). Neurogenetics, 18(1), 71. https://doi.org/10.1007/s10048-016-0503-3

@article{68082192f59c4180a40ecd2fafa33edf,

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

abstract = "The original version of this article inadvertently contained a mistake. The authors, editors and publisher confirmthat patient consent to publish the patient{\textquoteright}s photographs was obtained. This information was mistakenly omitted 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",

note = "Publisher Copyright: {\textcopyright} 2016,Springer-Verlag Berlin Heidelberg.",

year = "2017",

month = jan,

day = "1",

doi = "10.1007/s10048-016-0503-3",

language = "English (US)",

volume = "18",

pages = "71",

journal = "Neurogenetics",

issn = "1364-6745",

publisher = "Springer Science and Business Media Deutschland GmbH",

number = "1",

}

TY - JOUR

T1 - Erratum to

T2 - PARP10 deficiency manifests by severe developmental delay and DNA repair defect (Neurogenetics, (2016), 17, (227-232), 10.1007/s10048-016-0493-1)

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 - 2017/1/1

Y1 - 2017/1/1

N2 - The original version of this article inadvertently contained a mistake. The authors, editors and publisher confirmthat patient consent to publish the patient’s photographs was obtained. This information was mistakenly omitted in the original paper.

AB - The original version of this article inadvertently contained a mistake. The authors, editors and publisher confirmthat patient consent to publish the patient’s photographs was obtained. This information was mistakenly omitted in the original paper.

UR - https://www.scopus.com/pages/publications/85002002487

UR - https://www.scopus.com/pages/publications/85002002487#tab=citedBy

U2 - 10.1007/s10048-016-0503-3

DO - 10.1007/s10048-016-0503-3

M3 - Comment/debate

C2 - 27921172

AN - SCOPUS:85002002487

SN - 1364-6745

VL - 18

SP - 71

JO - Neurogenetics

JF - Neurogenetics

IS - 1

ER -

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

Abstract

All Science Journal Classification (ASJC) codes

Access to Document

Other files and links

Fingerprint

Cite this