Erratum: Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice (Human Molecular Genetics (2013) 22 (1026-1038) DOI: 10.1093/hmg/dds507)

Tyler F. Beck; Danielle Veenma; Oleg A. Shchelochkov; Zhiyin Yu; Bum Jun Kim; Hitisha P. Zaveri; Yolande Van Bever; Sunju Choi; Hannie Douben; Terry K. Bertin; Pragna I. Patel; Brendan Lee; Dick Tibboel; Annelies De Klein; David W. Stockton; Monica J. Justice; Daryl A. Scott

doi:10.1093/hmg/ddz307

Erratum: Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice (Human Molecular Genetics (2013) 22 (1026-1038) DOI: 10.1093/hmg/dds507)

Tyler F. Beck, Danielle Veenma, Oleg A. Shchelochkov, Zhiyin Yu, Bum Jun Kim, Hitisha P. Zaveri, Yolande Van Bever, Sunju Choi, Hannie Douben, Terry K. Bertin, Pragna I. Patel, Brendan Lee, Dick Tibboel, Annelies De Klein, David W. Stockton, Monica J. Justice, Daryl A. Scott

Research output: Contribution to journal › Comment/debate

Abstract

In the originally published version of this article it was indicated that the variant leading to the Frem1 allele was a c.2477T >A variant leading to p.Lys826∗. It is actually leads to a p.Leu826∗.

Original language	English
Pages (from-to)	1054
Number of pages	1
Journal	Human Molecular Genetics
Volume	29
Issue number	6
DOIs	https://doi.org/10.1093/hmg/ddz307
State	Published - Apr 15 2020

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Beck, T. F., Veenma, D., Shchelochkov, O. A., Yu, Z., Kim, B. J., Zaveri, H. P., Van Bever, Y., Choi, S., Douben, H., Bertin, T. K., Patel, P. I., Lee, B., Tibboel, D., De Klein, A., Stockton, D. W., Justice, M. J., & Scott, D. A. (2020). Erratum: Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice (Human Molecular Genetics (2013) 22 (1026-1038) DOI: 10.1093/hmg/dds507). Human Molecular Genetics, 29(6), 1054. https://doi.org/10.1093/hmg/ddz307

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title = "Erratum: Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice (Human Molecular Genetics (2013) 22 (1026-1038) DOI: 10.1093/hmg/dds507)",

abstract = "In the originally published version of this article it was indicated that the variant leading to the Frem1 allele was a c.2477T >A variant leading to p.Lys826∗. It is actually leads to a p.Leu826∗.",

author = "Beck, {Tyler F.} and Danielle Veenma and Shchelochkov, {Oleg A.} and Zhiyin Yu and Kim, {Bum Jun} and Zaveri, {Hitisha P.} and {Van Bever}, Yolande and Sunju Choi and Hannie Douben and Bertin, {Terry K.} and Patel, {Pragna I.} and Brendan Lee and Dick Tibboel and {De Klein}, Annelies and Stockton, {David W.} and Justice, {Monica J.} and Scott, {Daryl A.}",

year = "2020",

month = apr,

day = "15",

doi = "10.1093/hmg/ddz307",

language = "English",

volume = "29",

pages = "1054",

journal = "Human Molecular Genetics",

issn = "0964-6906",

number = "6",

}

Beck, TF, Veenma, D, Shchelochkov, OA, Yu, Z, Kim, BJ, Zaveri, HP, Van Bever, Y, Choi, S, Douben, H, Bertin, TK, Patel, PI, Lee, B, Tibboel, D, De Klein, A, Stockton, DW, Justice, MJ & Scott, DA 2020, 'Erratum: Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice (Human Molecular Genetics (2013) 22 (1026-1038) DOI: 10.1093/hmg/dds507)', Human Molecular Genetics, vol. 29, no. 6, pp. 1054. https://doi.org/10.1093/hmg/ddz307

Erratum : Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice (Human Molecular Genetics (2013) 22 (1026-1038) DOI: 10.1093/hmg/dds507). / Beck, Tyler F.; Veenma, Danielle; Shchelochkov, Oleg A. et al.

In: Human Molecular Genetics, Vol. 29, No. 6, 15.04.2020, p. 1054.

Research output: Contribution to journal › Comment/debate

TY - JOUR

T1 - Erratum

T2 - Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice (Human Molecular Genetics (2013) 22 (1026-1038) DOI: 10.1093/hmg/dds507)

AU - Beck, Tyler F.

AU - Veenma, Danielle

AU - Shchelochkov, Oleg A.

AU - Yu, Zhiyin

AU - Kim, Bum Jun

AU - Zaveri, Hitisha P.

AU - Van Bever, Yolande

AU - Choi, Sunju

AU - Douben, Hannie

AU - Bertin, Terry K.

AU - Patel, Pragna I.

AU - Lee, Brendan

AU - Tibboel, Dick

AU - De Klein, Annelies

AU - Stockton, David W.

AU - Justice, Monica J.

AU - Scott, Daryl A.

PY - 2020/4/15

Y1 - 2020/4/15

N2 - In the originally published version of this article it was indicated that the variant leading to the Frem1 allele was a c.2477T >A variant leading to p.Lys826∗. It is actually leads to a p.Leu826∗.

AB - In the originally published version of this article it was indicated that the variant leading to the Frem1 allele was a c.2477T >A variant leading to p.Lys826∗. It is actually leads to a p.Leu826∗.

UR - http://www.scopus.com/inward/record.url?scp=85083545348&partnerID=8YFLogxK

U2 - 10.1093/hmg/ddz307

DO - 10.1093/hmg/ddz307

M3 - Comment/debate

C2 - 32016392

AN - SCOPUS:85083545348

VL - 29

SP - 1054

JO - Human Molecular Genetics

JF - Human Molecular Genetics

SN - 0964-6906

IS - 6

ER -

Erratum: Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice (Human Molecular Genetics (2013) 22 (1026-1038) DOI: 10.1093/hmg/dds507)

Abstract

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