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T Lerman-Sagie

First name:
T
Last name:
Lerman-Sagie
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)
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)