Association of concomitant congenital diaphragmatic hernia and Hirschsprung's disease with a mutation in the FOXP1 gene: A case report
Introduction: Forkhead box protein P1 (FOXP1) is a transcriptional factor that plays a role in gene regulation in a wide array of human tissues. Mutations of this gene result in developmental delay, language deficits, brain, cardiac and urogenital anomalies. Some evidence also connects these mutatio...
Saved in:
| Main Authors: | , |
|---|---|
| Format: | Book |
| Published: |
Elsevier,
2024-07-01T00:00:00Z.
|
| Subjects: | |
| Online Access: | Connect to this object online. |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|