Biallelic NEXN variants and fetal onset dilated cardiomyopathy: two independent case reports and revision of literature

Abstract Background Dilated cardiomyopathy (DCM) is an etiologically heterogeneous group of diseases of the myocardium. With the rapid evolution in laboratory investigations, genetic background is increasingly determined including many genes with variable penetrance and expressivity. Biallelic NEXN...

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Hlavní autoři:	Irene Picciolli, Angelo Ratti, Berardo Rinaldi, Anwar Baban, Maria Iascone, Gaia Francescato, Alessia Cappelleri, Monia Magliozzi, Antonio Novelli, Giovanni Parlapiano, Anna Maria Colli, Nicola Persico, Stefano Carugo, Fabio Mosca, Maria Francesca Bedeschi
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	BMC 2024-08-01
Edice:	Italian Journal of Pediatrics
Témata:	Case reports Dilated cardiomyopathy (DCM) Hypertrophic cardiomyopathy (HCM) Nexilin NEXN
On-line přístup:	https://doi.org/10.1186/s13052-024-01678-x
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