Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability

S. Riazuddin; M. Hussain; A. Razzaq; Z. Iqbal; M. Shahzad; D.L. Polla; Y. Song; E. van Beusekom; A.A. Khan; L. Tomas-Roca; M. Rashid; M.Y. Zahoor; W.M. Wissink-Lindhout; M.A.R. Basra; M. Ansar; Z. Agha; K. van Heeswijk; F. Rasheed; M. Van de Vorst; J.A. Veltman; C. Gilissen; J. Akram; T. Kleefstra; M.Z. Assir; D. Grozeva; K. Carss; F.L. Raymond; T.D. O'Connor; S.A. Riazuddin; S.N. Khan; Z.M. Ahmed; A.P.M. de Brouwer; H. van Bokhoven; U.K.1.0.K. UK10K; UK10K

doi:10.1038/s41380-018-0128-z

Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability

S. Riazuddin^*, M. Hussain, A. Razzaq, Z. Iqbal, M. Shahzad, D.L. Polla, Y. Song, E. van Beusekom, A.A. Khan, L. Tomas-Roca, M. Rashid, M.Y. Zahoor, W.M. Wissink-Lindhout, M.A.R. Basra, M. Ansar, Z. Agha, K. van Heeswijk, F. Rasheed, M. Van de Vorst, J.A. VeltmanC. Gilissen, J. Akram, T. Kleefstra, M.Z. Assir, D. Grozeva, K. Carss, F.L. Raymond, T.D. O'Connor, S.A. Riazuddin, S.N. Khan, Z.M. Ahmed, A.P.M. de Brouwer, H. van Bokhoven^*, U.K.1.0.K. UK10K, UK10K

^*Corresponding author for this work

GROW - Reproductive and Perinatal Medicine

Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

Abstract

This Article was originally published under a CC BY-NC-SA 4.0 license, but has now been made available under a CC BY 4.0 license. The PDF and HTML versions of the Article have been modified accordingly.

Original language	English
Pages (from-to)	3101-3102
Number of pages	2
Journal	Molecular Psychiatry
Volume	25
Issue number	11
DOIs	https://doi.org/10.1038/s41380-018-0128-z
Publication status	Published - 1 Nov 2020

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10.1038/s41380-018-0128-zLicence: CC BY-NC-SA

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Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability
Riazuddin, S., Hussain, M., Razzaq, A., Iqbal, Z., Shahzad, M., Polla, D. L., Song, Y., van Beusekom, E., Khan, A. A., Tomas-Roca, L., Rashid, M., Zahoor, M. Y., Wissink-Lindhout, W. M., Basra, M. A. R., Ansar, M., Agha, Z., van Heeswijk, K., Rasheed, F., Van de Vorst, M., Veltman, J. A., & 15 othersGilissen, C., Akram, J., Kleefstra, T., Assir, M. Z., Grozeva, D., Carss, K., Raymond, F. L., O'Connor, T. D., Riazuddin, S. A., Khan, S. N., Ahmed, Z. M., de Brouwer, A. P. M., van Bokhoven, H., Riazuddin, S. & UK10K, Nov 2017, In: Molecular Psychiatry. 22, 11, p. 1604-1614 11 p.
Research output: Contribution to journal › Article › Academic › peer-review

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Riazuddin, S., Hussain, M., Razzaq, A., Iqbal, Z., Shahzad, M., Polla, D. L., Song, Y., van Beusekom, E., Khan, A. A., Tomas-Roca, L., Rashid, M., Zahoor, M. Y., Wissink-Lindhout, W. M., Basra, M. A. R., Ansar, M., Agha, Z., van Heeswijk, K., Rasheed, F., Van de Vorst, M., ... UK10K (2020). Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability. Molecular Psychiatry, 25(11), 3101-3102. https://doi.org/10.1038/s41380-018-0128-z

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title = "Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability",

abstract = "This Article was originally published under a CC BY-NC-SA 4.0 license, but has now been made available under a CC BY 4.0 license. The PDF and HTML versions of the Article have been modified accordingly.",

author = "S. Riazuddin and M. Hussain and A. Razzaq and Z. Iqbal and M. Shahzad and D.L. Polla and Y. Song and {van Beusekom}, E. and A.A. Khan and L. Tomas-Roca and M. Rashid and M.Y. Zahoor and W.M. Wissink-Lindhout and M.A.R. Basra and M. Ansar and Z. Agha and {van Heeswijk}, K. and F. Rasheed and {Van de Vorst}, M. and J.A. Veltman and C. Gilissen and J. Akram and T. Kleefstra and M.Z. Assir and D. Grozeva and K. Carss and F.L. Raymond and T.D. O'Connor and S.A. Riazuddin and S.N. Khan and Z.M. Ahmed and {de Brouwer}, A.P.M. and {van Bokhoven}, H. and U.K.1.0.K. UK10K and UK10K",

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doi = "10.1038/s41380-018-0128-z",

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Riazuddin, S, Hussain, M, Razzaq, A, Iqbal, Z, Shahzad, M, Polla, DL, Song, Y, van Beusekom, E, Khan, AA, Tomas-Roca, L, Rashid, M, Zahoor, MY, Wissink-Lindhout, WM, Basra, MAR, Ansar, M, Agha, Z, van Heeswijk, K, Rasheed, F, Van de Vorst, M, Veltman, JA, Gilissen, C, Akram, J, Kleefstra, T, Assir, MZ, Grozeva, D, Carss, K, Raymond, FL, O'Connor, TD, Riazuddin, SA, Khan, SN, Ahmed, ZM, de Brouwer, APM, van Bokhoven, H, UK10K, UKK & UK10K 2020, 'Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability', Molecular Psychiatry, vol. 25, no. 11, pp. 3101-3102. https://doi.org/10.1038/s41380-018-0128-z

TY - JOUR

T1 - Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability

AU - Riazuddin, S.

AU - Hussain, M.

AU - Razzaq, A.

AU - Iqbal, Z.

AU - Shahzad, M.

AU - Polla, D.L.

AU - Song, Y.

AU - van Beusekom, E.

AU - Khan, A.A.

AU - Tomas-Roca, L.

AU - Rashid, M.

AU - Zahoor, M.Y.

AU - Wissink-Lindhout, W.M.

AU - Basra, M.A.R.

AU - Ansar, M.

AU - Agha, Z.

AU - van Heeswijk, K.

AU - Rasheed, F.

AU - Van de Vorst, M.

AU - Veltman, J.A.

AU - Gilissen, C.

AU - Akram, J.

AU - Kleefstra, T.

AU - Assir, M.Z.

AU - Grozeva, D.

AU - Carss, K.

AU - Raymond, F.L.

AU - O'Connor, T.D.

AU - Riazuddin, S.A.

AU - Khan, S.N.

AU - Ahmed, Z.M.

AU - de Brouwer, A.P.M.

AU - van Bokhoven, H.

AU - UK10K, U.K.1.0.K.

AU - UK10K

PY - 2020/11/1

Y1 - 2020/11/1

N2 - This Article was originally published under a CC BY-NC-SA 4.0 license, but has now been made available under a CC BY 4.0 license. The PDF and HTML versions of the Article have been modified accordingly.

AB - This Article was originally published under a CC BY-NC-SA 4.0 license, but has now been made available under a CC BY 4.0 license. The PDF and HTML versions of the Article have been modified accordingly.

U2 - 10.1038/s41380-018-0128-z

DO - 10.1038/s41380-018-0128-z

M3 - Erratum / corrigendum / retractions

C2 - 30171209

SN - 1359-4184

VL - 25

SP - 3101

EP - 3102

JO - Molecular Psychiatry

JF - Molecular Psychiatry

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