Varaico: Literature-Extracted Genetic Variants

Gene:FOXF1
Variant:p.F77L
Back to variants list

FOXF1

NM_001451.3:p.F77L

Associated Papers

Genetic burden in neonatal and pediatric-onset pulmonary hypertension: A single-center retrospective study using exome sequencing in a Chinese population.

Chen C et al.

Pediatrics and Neonatology, 2025

Familial Alveolar Capillary Dysplasia With Misalignment of Pulmonary Veins Caused by Paternal FOXF1 Upstream Enhancer Deletion: A Case Report.

Kawasaki H et al.

American Journal of Medical Genetics. Part A, 2025

Variable phenotypic presentation of a novel FOXF1 missense mutation in a single family.

Reiter J et al.

Pediatric Pulmonology, 2016

Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veins.

Szafranski P et al.

Human Genetics, 2016

Alveolar capillary dysplasia with misalignment of the pulmonary veins: clinical, histological, and genetic aspects.

Slot E et al.

Pulmonary Circulation, 0

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."