FBN1 c.737-25C>T

Variant ID: 15-48826427-G-A

NM_000138.4(FBN1):c.737-25C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Next-generation sequencing identifies novel mutations in the FBN1 gene for two Chinese families with Marfan syndrome.

Molecular Medicine Reports
Ma, Mingjia M; Li, Zongzhe Z; Wang, Dao Wen DW; Wei, Xiang X
Publication Date: 2016-07

Variant appearance in text: rs3837725
PubMed Link: 27175573
Variant Present in the following documents:
  • Main text
  • mmr-14-01-0151.pdf
View BVdb publication page