Correction to: Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta (Journal of Biomedical Science (2018) 25 (82) DOI: 10.1186/s12929-018-0481-x)

Mehran Kausar; Saima Siddiqi; Muhammad Yaqoob; Sajid Mansoor; Outi Makitie; Asif Mir; Chiea Chuen Khor; Jia Nee Foo; Mariam Anees

doi:10.1186/s12929-019-0525-x

Correction to: Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta (Journal of Biomedical Science (2018) 25 (82) DOI: 10.1186/s12929-018-0481-x)

Mehran Kausar, Saima Siddiqi, Muhammad Yaqoob, Sajid Mansoor, Outi Makitie, Asif Mir, Chiea Chuen Khor, Jia Nee Foo^*, Mariam Anees

^*Corresponding author for this work

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

1 Citation (Scopus)

Abstract

In the original publication of this article [1], there are two errors in the article which the cDNA position of the pathogenic variant WNT1 p.Gly324Cys should be c.970G>T instead of c.1168G>T.

Original language	English
Article number	31
Journal	Journal of Biomedical Science
Volume	26
Issue number	1
DOIs	https://doi.org/10.1186/s12929-019-0525-x
Publication status	Published - Apr 28 2019
Externally published	Yes

Bibliographical note

Publisher Copyright:
© 2019 The Author(s).

ASJC Scopus Subject Areas

Endocrinology, Diabetes and Metabolism
Molecular Biology
Clinical Biochemistry
Cell Biology
Biochemistry, medical
Pharmacology (medical)

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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Kausar, M., Siddiqi, S., Yaqoob, M., Mansoor, S., Makitie, O., Mir, A., Khor, C. C., Foo, J. N., & Anees, M. (2019). Correction to: Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta (Journal of Biomedical Science (2018) 25 (82) DOI: 10.1186/s12929-018-0481-x). Journal of Biomedical Science, 26(1), Article 31. https://doi.org/10.1186/s12929-019-0525-x

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title = "Correction to: Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta (Journal of Biomedical Science (2018) 25 (82) DOI: 10.1186/s12929-018-0481-x)",

abstract = "In the original publication of this article [1], there are two errors in the article which the cDNA position of the pathogenic variant WNT1 p.Gly324Cys should be c.970G>T instead of c.1168G>T.",

author = "Mehran Kausar and Saima Siddiqi and Muhammad Yaqoob and Sajid Mansoor and Outi Makitie and Asif Mir and Khor, {Chiea Chuen} and Foo, {Jia Nee} and Mariam Anees",

note = "Publisher Copyright: {\textcopyright} 2019 The Author(s).",

year = "2019",

month = apr,

day = "28",

doi = "10.1186/s12929-019-0525-x",

language = "English",

volume = "26",

journal = "Journal of Biomedical Science",

issn = "1021-7770",

publisher = "BioMed Central",

number = "1",

}

Kausar, M, Siddiqi, S, Yaqoob, M, Mansoor, S, Makitie, O, Mir, A, Khor, CC, Foo, JN & Anees, M 2019, 'Correction to: Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta (Journal of Biomedical Science (2018) 25 (82) DOI: 10.1186/s12929-018-0481-x)', Journal of Biomedical Science, vol. 26, no. 1, 31. https://doi.org/10.1186/s12929-019-0525-x

Correction to: Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta (Journal of Biomedical Science (2018) 25 (82) DOI: 10.1186/s12929-018-0481-x). / Kausar, Mehran; Siddiqi, Saima; Yaqoob, Muhammad et al.
In: Journal of Biomedical Science, Vol. 26, No. 1, 31, 28.04.2019.

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

TY - JOUR

T1 - Correction to

T2 - Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta (Journal of Biomedical Science (2018) 25 (82) DOI: 10.1186/s12929-018-0481-x)

AU - Kausar, Mehran

AU - Siddiqi, Saima

AU - Yaqoob, Muhammad

AU - Mansoor, Sajid

AU - Makitie, Outi

AU - Mir, Asif

AU - Khor, Chiea Chuen

AU - Foo, Jia Nee

AU - Anees, Mariam

PY - 2019/4/28

Y1 - 2019/4/28

N2 - In the original publication of this article [1], there are two errors in the article which the cDNA position of the pathogenic variant WNT1 p.Gly324Cys should be c.970G>T instead of c.1168G>T.

AB - In the original publication of this article [1], there are two errors in the article which the cDNA position of the pathogenic variant WNT1 p.Gly324Cys should be c.970G>T instead of c.1168G>T.

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UR - http://www.scopus.com/inward/citedby.url?scp=85065043471&partnerID=8YFLogxK

U2 - 10.1186/s12929-019-0525-x

DO - 10.1186/s12929-019-0525-x

M3 - Comment/debate

C2 - 31030663

AN - SCOPUS:85065043471

SN - 1021-7770

VL - 26

JO - Journal of Biomedical Science

JF - Journal of Biomedical Science

IS - 1

M1 - 31

ER -

Correction to: Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta (Journal of Biomedical Science (2018) 25 (82) DOI: 10.1186/s12929-018-0481-x)

Abstract

Bibliographical note

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UN SDGs

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