@article{schmid:hal-04164127,
TITLE = {LHX2 haploinsufficiency causes a variable neurodevelopmental disorder},
AUTHOR = {Schmid, Cosima and Gregor, Anne and Costain, Gregory and Morel, Chantal and Massingham, Lauren and Schwab, Jennifer and Qu{\'e}lin, Chlo{\'e} and Faoucher, Marie and Kaplan, Julie and Procopio, Rebecca and Saunders, Carol and Cohen, Ana and Lemire, Gabrielle and Sacharow, Stephanie and O'Donnell-Luria, Anne and Segal, Ranit Jaron and Kianmahd Shamshoni, Jessica and Schweitzer, Daniela and Ebrahimi-Fakhari, Darius and Monaghan, Kristin and Palculict, Timothy Blake and Napier, Melanie and Tao, Alice and Isidor, Bertrand and Moradkhani, Kamran and Reis, Andr{\'e} and Sticht, Heinrich and Chung, Wendy and Zweier, Christiane},
URL = {https://univ-rennes.hal.science/hal-04164127},
JOURNAL = {Genetics in Medicine},
PUBLISHER = {Nature Publishing Group},
VOLUME = {25},
NUMBER = {7},
PAGES = {100839},
YEAR = {2023},
MONTH = Jul, DOI = {10.1016/j.gim.2023.100839},
KEYWORDS = {ASD ; Intellectual disability ; LHX2 ; Microcephaly ; NDD ; Neurodevelopmental disorder},
HAL_ID = {hal-04164127},
HAL_VERSION = {v1},
}