Correction: DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients (European Journal of Human Genetics, (2020), 28, 1, (64-75), 10.1038/s41431-019-0374-9)

Roser Urreizti; Klaus Mayer; Gilad D. Evrony; Edith Said; Laura Castilla-Vallmanya; Neal A.L. Cody; Guillem Plasencia; Bruce D. Gelb; Daniel Grinberg; Ulrich Brinkmann; Bryn D. Webb; Susanna Balcells

doi:10.1038/s41431-019-0394-5

Correction: DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients (European Journal of Human Genetics, (2020), 28, 1, (64-75), 10.1038/s41431-019-0374-9)

Roser Urreizti, Klaus Mayer, Gilad D. Evrony, Edith Said, Laura Castilla-Vallmanya, Neal A.L. Cody, Guillem Plasencia, Bruce D. Gelb, Daniel Grinberg, Ulrich Brinkmann, Bryn D. Webb, Susanna Balcells

Research output: Contribution to journal › Comment/debate

Abstract

Following the publication of the article, it was noted that the last column in Table 1, the total % should have read 5/8 (62.5) for the ‘Epilepsy’ row, and not 5.7 (71.4). This has now been amended in the HTML and PDF of the original article.

Original language	English
Pages (from-to)	138
Number of pages	1
Journal	European Journal of Human Genetics
Volume	28
Issue number	1
DOIs	https://doi.org/10.1038/s41431-019-0394-5
State	Published - 1 Jan 2020

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Urreizti, R., Mayer, K., Evrony, G. D., Said, E., Castilla-Vallmanya, L., Cody, N. A. L., Plasencia, G., Gelb, B. D., Grinberg, D., Brinkmann, U., Webb, B. D., & Balcells, S. (2020). Correction: DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients (European Journal of Human Genetics, (2020), 28, 1, (64-75), 10.1038/s41431-019-0374-9). European Journal of Human Genetics, 28(1), 138. https://doi.org/10.1038/s41431-019-0394-5

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title = "Correction: DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients (European Journal of Human Genetics, (2020), 28, 1, (64-75), 10.1038/s41431-019-0374-9)",

abstract = "Following the publication of the article, it was noted that the last column in Table 1, the total % should have read 5/8 (62.5) for the {\textquoteleft}Epilepsy{\textquoteright} row, and not 5.7 (71.4). This has now been amended in the HTML and PDF of the original article.",

author = "Roser Urreizti and Klaus Mayer and Evrony, {Gilad D.} and Edith Said and Laura Castilla-Vallmanya and Cody, {Neal A.L.} and Guillem Plasencia and Gelb, {Bruce D.} and Daniel Grinberg and Ulrich Brinkmann and Webb, {Bryn D.} and Susanna Balcells",

note = "Publisher Copyright: {\textcopyright} 2019, European Society of Human Genetics.",

year = "2020",

month = jan,

day = "1",

doi = "10.1038/s41431-019-0394-5",

language = "English",

volume = "28",

pages = "138",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

publisher = "Nature Publishing Group",

number = "1",

}

Urreizti, R, Mayer, K, Evrony, GD, Said, E, Castilla-Vallmanya, L, Cody, NAL, Plasencia, G, Gelb, BD, Grinberg, D, Brinkmann, U, Webb, BD & Balcells, S 2020, 'Correction: DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients (European Journal of Human Genetics, (2020), 28, 1, (64-75), 10.1038/s41431-019-0374-9)', European Journal of Human Genetics, vol. 28, no. 1, pp. 138. https://doi.org/10.1038/s41431-019-0394-5

Correction: DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients (European Journal of Human Genetics, (2020), 28, 1, (64-75), 10.1038/s41431-019-0374-9). / Urreizti, Roser; Mayer, Klaus; Evrony, Gilad D. et al.
In: European Journal of Human Genetics, Vol. 28, No. 1, 01.01.2020, p. 138.

Research output: Contribution to journal › Comment/debate

TY - JOUR

T1 - Correction

T2 - DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients (European Journal of Human Genetics, (2020), 28, 1, (64-75), 10.1038/s41431-019-0374-9)

AU - Urreizti, Roser

AU - Mayer, Klaus

AU - Evrony, Gilad D.

AU - Said, Edith

AU - Castilla-Vallmanya, Laura

AU - Cody, Neal A.L.

AU - Plasencia, Guillem

AU - Gelb, Bruce D.

AU - Grinberg, Daniel

AU - Brinkmann, Ulrich

AU - Webb, Bryn D.

AU - Balcells, Susanna

PY - 2020/1/1

Y1 - 2020/1/1

N2 - Following the publication of the article, it was noted that the last column in Table 1, the total % should have read 5/8 (62.5) for the ‘Epilepsy’ row, and not 5.7 (71.4). This has now been amended in the HTML and PDF of the original article.

AB - Following the publication of the article, it was noted that the last column in Table 1, the total % should have read 5/8 (62.5) for the ‘Epilepsy’ row, and not 5.7 (71.4). This has now been amended in the HTML and PDF of the original article.

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U2 - 10.1038/s41431-019-0394-5

DO - 10.1038/s41431-019-0394-5

M3 - Comment/debate

C2 - 31477843

AN - SCOPUS:85076447111

SN - 1018-4813

VL - 28

SP - 138

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 1

ER -

Urreizti R, Mayer K, Evrony GD, Said E, Castilla-Vallmanya L, Cody NAL et al. Correction: DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients (European Journal of Human Genetics, (2020), 28, 1, (64-75), 10.1038/s41431-019-0374-9). European Journal of Human Genetics. 2020 Jan 1;28(1):138. doi: 10.1038/s41431-019-0394-5