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High-Throughput Genomics Identify Novel FBN1/2 Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects.

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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
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ISSN:16616596
DOI:10.3390/ijms25105469