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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author Casey Thornton
Elizabeth Mizerik
Dan Brooks
Chaya Murali
Christian Parobek
Lorraine Potocki
Pengfei Liu
Nichole Owen
Liesbeth Vossaert
author_facet Casey Thornton
Elizabeth Mizerik
Dan Brooks
Chaya Murali
Christian Parobek
Lorraine Potocki
Pengfei Liu
Nichole Owen
Liesbeth Vossaert
author_sort Casey Thornton
collection DOAJ
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issn 2949-7744
language English
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publishDate 2023-01-01
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spelling doaj.art-9cd2d28a0eeb413c978fc3bf692f74552024-01-27T07:09:54ZengElsevierGenetics in Medicine Open2949-77442023-01-0111100620P573: Biallelic missense NEXN variants lead to recessive severe neonatal cardiomyopathyCasey Thornton0Elizabeth Mizerik1Dan Brooks2Chaya Murali3Christian Parobek4Lorraine Potocki5Pengfei Liu6Nichole Owen7Liesbeth Vossaert8Baylor College of Medicine, Houston, TX; Baylor Genetics, Houston, TXBaylor College of Medicine, Houston, TX; Texas Children Hospital, Houston, TXBaylor College of Medicine, Houston, TXBaylor College of Medicine, Houston, TX; Texas Children Hospital, Houston, TXBaylor College of Medicine, Houston, TXBaylor College of Medicine, Houston, TX; Texas Children Hospital, Houston, TXBaylor College of Medicine, Houston, TX; Baylor Genetics, Houston, TXBaylor College of Medicine, Houston, TX; Baylor Genetics, Houston, TXBaylor College of Medicine, Houston, TX; Baylor Genetics, Houston, TXhttp://www.sciencedirect.com/science/article/pii/S2949774423006209
spellingShingle Casey Thornton
Elizabeth Mizerik
Dan Brooks
Chaya Murali
Christian Parobek
Lorraine Potocki
Pengfei Liu
Nichole Owen
Liesbeth Vossaert
P573: Biallelic missense NEXN variants lead to recessive severe neonatal cardiomyopathy
Genetics in Medicine Open
title P573: Biallelic missense NEXN variants lead to recessive severe neonatal cardiomyopathy
title_full P573: Biallelic missense NEXN variants lead to recessive severe neonatal cardiomyopathy
title_fullStr P573: Biallelic missense NEXN variants lead to recessive severe neonatal cardiomyopathy
title_full_unstemmed P573: Biallelic missense NEXN variants lead to recessive severe neonatal cardiomyopathy
title_short P573: Biallelic missense NEXN variants lead to recessive severe neonatal cardiomyopathy
title_sort p573 biallelic missense nexn variants lead to recessive severe neonatal cardiomyopathy
url http://www.sciencedirect.com/science/article/pii/S2949774423006209
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