Schmid, C. M., Gregor, A., Costain, G., Morel, C. F., Massingham, L., Schwab, J., Quélin, C., Faoucher, M., Kaplan, J., Procopio, R., Saunders, C. J., Cohen, A. S. A., Lemire, G., Sacharow, S., O’Donnell-Luria, A., Segal, R. J., Kianmahd Shamshoni, J., Schweitzer, D., Ebrahimi-Fakhari, D., … Zweier, C. (2023). LHX2 haploinsufficiency causes a variable neurodevelopmental disorder. Genetics in Medicine, 25(7), 100839. https://doi.org/10.1016/j.gim.2023.100839
Columbia Affiliation:
Subjects:
Publication Type:
Article
Unique ID:
10.1016/j.gim.2023.100839
PMID:
Journal:
Publication Date:
Data Source:
PubMed
Source Link: