Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome

Authors

Marjolein J.A. Weerts, Erasmus University Rotterdam
Kristina Lanko, Erasmus University Rotterdam
Francisco J. Guzmán-Vega, King Abdullah University of Science and Technology
Adam Jackson, Manchester University NHS Foundation Trust
Reshmi Ramakrishnan, King Abdullah University of Science and Technology
Kelly J. Cardona-Londoño, King Abdullah University of Science and Technology
Karla A. Peña-Guerra, King Abdullah University of Science and Technology
Bever Y van
Paassen BW van
Anneke Kievit, Erasmus University Rotterdam
Slegtenhorst M van
Nicholas M. Allen, University of Galway
Caroline M. Kehoe, University of Galway
Hannah K. Robinson, Royal Devon & Exeter NHS Foundation Trust
Lewis Pang, Royal Devon & Exeter NHS Foundation Trust
Selina H. Banu, Dr. M.R. Khan Shishu (Children) Hospital and ICH
Mashaya Zaman, Dr. M.R. Khan Shishu (Children) Hospital and ICH
Stephanie Efthymiou, University College London
Henry Houlden, University College London
Irma Järvelä, University of Helsinki
Leena Lauronen, University of Helsinki
Tuomo Määttä, Joint Authority for Kainuu
Isabelle Schrauwen, Columbia University
Suzanne M. Leal, Columbia University
Claudia A.L. Ruivenkamp, Leiden University
Daniela Q.C.M. Barge-Schaapveld, Leiden University
Cacha M.P.C.D. Peeters-Scholte, Leiden University
Hamid Galehdari, Shahid Chamran University of Ahvaz
Neda Mazaheri, Shahid Chamran University of Ahvaz
Sanjay M. Sisodiya, Chalfont Centre for Epilepsy

DOI

10.1038/s41436-021-01246-2

Publication Date

2021-01-01

Publication Title

Genetics in Medicine

Volume

23

Issue

11

ISSN

1098-3600

Embargo Period

9999-12-31

First Page

2122

Last Page

2137

Recommended Citation

Weerts, M., Lanko, K., Guzmán-Vega, F., Jackson, A., Ramakrishnan, R., Cardona-Londoño, K., Peña-Guerra, K., van, B., van, P., Kievit, A., van, S., Allen, N., Kehoe, C., Robinson, H., Pang, L., Banu, S., Zaman, M., Efthymiou, S., Houlden, H., Järvelä, I., Lauronen, L., Määttä, T., Schrauwen, I., Leal, S., Ruivenkamp, C., Barge-Schaapveld, D., Peeters-Scholte, C., Galehdari, H., Mazaheri, N., & Sisodiya, S. (2021) 'Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome', Genetics in Medicine, 23(11), pp. 2122-2137. Available at: 10.1038/s41436-021-01246-2" >https://doi.org/10.1038/s41436-021-01246-2