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  4. Long QT syndrome and left ventricular non-compaction in a family with KCNH2 mutation: A case report
 
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Long QT syndrome and left ventricular non-compaction in a family with KCNH2 mutation: A case report

Journal
Frontiers in Pediatrics
Author(s)
Caiffa Thomas 
Antimo Tessitore
Loira Leoni
Elena Reffo
Chicco Daniela
D'Agata Mottolese Biancamaria 
Rubinato Elisa 
Girotto Giorgia 
Lenarduzzi Stefania
Barbi Egidio 
Bobbo Marco 
Giovanni Di Salvo
DOI
10.3389/fped.2022.970240
Project(s)
A unique cohort to study mechanisms underlying sex differences in cardiometabolic diseases 
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C.A.R.S.O. - I.R.C.C.S. materno infantile Burlo Garofolo

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