FBN1
Type: Concept
As of November 2026, FBN1 has been mentioned in one podcast episode on Osmosis from Elsevier (Jan 2026).
A gene that encodes the protein fibrillin-1, mutations of which are associated with Marfan syndrome.
| Mentioned in | 1 episode on 1 podcast (as of November 2026) |
|---|---|
| First heard | Jan 2026 on Osmosis from Elsevier |
Who talks about FBN1 on podcasts?
FBN1 came up; the most recent mention was Jan 2026 on Osmosis from Elsevier.
What is FBN1 mentioned alongside?
FBN1 is most often mentioned alongside primary ciliary dyskinesia, Marfan syndrome and Cartagena syndrome.
Mentioned together: primary ciliary dyskinesia, Marfan syndrome, Cartagena syndrome, alpha-1 antitrypsin deficiency