High-Throughput Genomics Identify Novel FBN1/2 Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects.
Saved in:
| Title: | High-Throughput Genomics Identify Novel FBN1/2 Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects. |
|---|---|
| Authors: | Zodanu, Gloria K. E.1,2 (AUTHOR) gzodanu@mednet.ucla.edu, Hwang, John H.1,2 (AUTHOR) gsatou@mednet.ucla.edu, Mehta, Zubin1,2 (AUTHOR) nhalnon@mednet.ucla.edu, Sisniega, Carlos1,2 (AUTHOR) csisniega@mednet.ucla.edu, Barsegian, Alexander1,2 (AUTHOR) barsegian88@gmail.com, Kang, Xuedong1,2 (AUTHOR) snelson@mednet.ucla.edu, Biniwale, Reshma2,3 (AUTHOR) msi@mednet.ucla.edu, Si, Ming-Sing3 (AUTHOR), Satou, Gary M.2 (AUTHOR), Halnon, Nancy2 (AUTHOR), Grody, Wayne W.2,4,5 (AUTHOR), Van Arsdell, Glen S.2,3 (AUTHOR), Nelson, Stanley F.2,4,5 (AUTHOR), Touma, Marlin1,2,6,7,8,9 (AUTHOR) mtouma@mednet.ucla.edu |
| Source: | International Journal of Molecular Sciences. May2024, Vol. 25 Issue 10, p5469. 15p. |
| Database: | Academic Search Ultimate |
|
Full text is not displayed to guests.
Login for full access.
|
|
Be the first to leave a comment!
