LHX2 haploinsufficiency causes a variable neurodevelopmental disorder

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
Authors:
Cosima M Schmid
Anne Gregor
Gregory Costain
Chantal F Morel
Lauren Massingham
Jennifer Schwab
Chloé Quélin
Marie Faoucher
Julie Kaplan
Rebecca Procopio
Carol J Saunders
Ana S A Cohen
Gabrielle Lemire
Stephanie Sacharow
Anne O'Donnell-Luria
Ranit Jaron Segal
Jessica Kianmahd Shamshoni
Daniela Schweitzer
Darius Ebrahimi-Fakhari
Kristin Monaghan
Timothy Blake Palculict
Melanie P Napier
Alice Tao
Bertrand Isidor
Kamran Moradkhani
André Reis
Heinrich Sticht
Wendy K Chung
Christiane Zweier
Affiliated Authors:
Alice Tao
Wendy K Chung
Author Keywords:
asd
intellectual disability
lhx2
microcephaly
ndd
neurodevelopmental disorder
Publication Type:
Article
Unique ID:
10.1016/j.gim.2023.100839
PMID:
Publication Date:
Data Source:
PubMed

Record Created: