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Paper Details

Heterozygous variants that disturb the transcriptional repressor activity of FOXP4 cause a developmental disorder with speech/language delays and multiple congenital abnormalities.
Genet Med
15
2021
FOXP genes, FOXP4, Luciferase, autosomal dominant neurodevelopmental disorder, cervical spine abnormalities, congenital abnormalities, congenital diaphragmatic hernia, developmental disorder, developmental disorders, forkhead box DNA-binding domain, growth abnormalities, growth defects, ptosis, speech and language delays, speech/language delays
Author NameAffiliation
Wendy K ChungColumbia University Irving Medical Center
Wendy K ChungColumbia University Irving Medical Center
Han G BrunnerRadboud University Medical Center
Han G BrunnerDonders Institute for Brain, Radboud University Medical Center
Han G BrunnerMaastricht University Medical Center
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