P573: Biallelic missense NEXN variants lead to recessive severe neonatal cardiomyopathy

P573: Biallelic missense NEXN variants lead to recessive severe neonatal cardiomyopathy

Bibliographic Details
Main Authors:	Casey Thornton, Elizabeth Mizerik, Dan Brooks, Chaya Murali, Christian Parobek, Lorraine Potocki, Pengfei Liu, Nichole Owen, Liesbeth Vossaert
Format:	Article
Language:	English
Published:	Elsevier 2023-01-01
Series:	Genetics in Medicine Open
Online Access:	http://www.sciencedirect.com/science/article/pii/S2949774423006209

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