P573: Biallelic missense NEXN variants lead to recessive severe neonatal cardiomyopathy
Main Authors: | , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2023-01-01
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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 |
first_indexed | 2024-03-08T10:26:49Z |
format | Article |
id | doaj.art-9cd2d28a0eeb413c978fc3bf692f7455 |
institution | Directory Open Access Journal |
issn | 2949-7744 |
language | English |
last_indexed | 2024-03-08T10:26:49Z |
publishDate | 2023-01-01 |
publisher | Elsevier |
record_format | Article |
series | Genetics in Medicine Open |
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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