Associated Papers
FOXJ1 Variants Causing Primary Ciliary Dyskinesia with Hydrocephalus: A Case Report from Japan.
Ito M et al.
Internal Medicine (tokyo, Japan), 2024
Novel dominant-negative FOXJ1 mutation in a family with heterotaxy plus mouse model.
Li L et al.
Translational Pediatrics, 2023
Congenital heart defects caused by FOXJ1.
Padua MB et al.
Human Molecular Genetics, 2023
Autosomal dominant variants in FOXJ1 causing primary ciliary dyskinesia in two patients with obstructive hydrocephalus.
Shapiro AJ et al.
Molecular Genetics & Genomic Medicine, 2021
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