Leibovitz, Z., Mandel, H., Falik-Zaccai, T., Ben Harouch, S., Savitzki, D., Krajden-Haratz, K., … Lerman-Sagie, T. (2017). Walker-Warburg syndrome and tectocerebellar dysraphia: A novel association caused by a homozygous DAG1 mutation. European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society. https://doi.org/10.1016/j.ejpn.2017.12.012 (Original work published 2017)
T Lerman-Sagie
First name:
T
Last name:
Lerman-Sagie
Fry, A., Fawcett, K., Zelnik, N., Yuan, H., Thompson, B., Shemer-Meiri, L., … Pilz, D. (2018). De novo mutations in GRIN1 cause extensive bilateral polymicrogyria. Brain : A Journal of Neurology. https://doi.org/10.1093/brain/awx358 (Original work published 2018)