MGA-related syndrome: A proposed novel disorder

MGA-related syndrome: A proposed novel disorder

Summary: MGA (OMIM: 616061) encodes a dual-specificity transcription factor that regulates the expression of Max-network and T-box family target genes, important in embryogenesis. Previous studies have linked MGA to various phenotypes, including neurodevelopmental disorders, congenital heart disease...

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Bibliographic Details
Main Authors:	Bobbi McGivern, Michelle M. Morrow, Erin Torti, Kirsty McWalter, Ingrid M. Wentzensen, Kristin G. Monaghan, Amanda Gerard, Laurie Robak, David Chitayat, Claire Botsford, Sarah Jurgensmeyer, Peter Leahy, Paul Kruszka
Format:	Article
Language:	English
Published:	Elsevier 2025-01-01
Series:	HGG Advances
Subjects:	MGA clinical exome sequencing candidate gene gene discovery congenital anomalies neurodevelopmental disorder
Online Access:	http://www.sciencedirect.com/science/article/pii/S2666247724001271
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