Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.
Document Type
Journal Article
Publication Date
4-19-2021
Journal
Genome Medicine
Volume
13
Issue
1
Inclusive Pages
63
DOI
10.1186/s13073-021-00870-6
APA Citation
Gillentine, M., Wang, T., Hoekzema, K., Rosenfeld, J., Liu, P., Guo, H., Kim, C., De Vries, B., Vissers, L., Nordenskjold, M., Kvarnung, M., Lindstrand, A., Nordgren, A., Gecz, J., Iascone, M., Cereda, A., Scatigno, A., Maitz, S., Zanni, G., Bertini, E., Zweier, C., Schuhmann, S., Wiesener, A., Pepper, M., Panjwani, H., Torti, E., Abid, F., Anselm, I., Srivastava, S., Atwal, P., Bacino, C., Bhat, G., Cobian, K., Bird, L., Friedman, J., Wright, M., Callewaert, B., Petit, F., Mathieu, S., Afenjar, A., Christensen, C., White, K., Elpeleg, O., Berger, I., Espineli, E., Fagerberg, C., Brasch-Andersen, C., Hansen, L., Feyma, T., Hughes, S., Thiffault, I., Sullivan, B., Yan, S., Keller, K., Keren, B., Mignot, C., Kooy, F., Meuwissen, M., Basinger, A., Kukolich, M., Philips, M., Ortega, L., Drummond-Borg, M., Lauridsen, M., Sorensen, K., Lehman, A., Lopez-Rangel, E., Levy, P., Lessel, D., Lotze, T., Madan-Khetarpal, S., Sebastian, J., Vento, J., Vats, D., Benman, L., Mckee, S., Mirzaa, G., Muss, C., Pappas, J., Peeters, H., Romano, C., Elia, M., Galesi, O., Simon, M., van Gassen, K., Simpson, K., Stratton, R., Syed, S., Thevenon, J., Palafoll, I., Vitobello, A., Bournez, M., Faivre, L., Xia, K., Earl, R., Nowakowski, T., Bernier, R., & Eichler, E. (2021). Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.. Genome Medicine, 13 (1). http://dx.doi.org/10.1186/s13073-021-00870-6
Peer Reviewed
1
Open Access
1
