Associated Papers
Nexilin in cardiomyopathy: unveiling its diverse roles with special focus on endocardial fibroelastosis.
Rahimzadeh M et al.
Heart Failure Reviews, 2024
Biallelic NEXN variants and fetal onset dilated cardiomyopathy: two independent case reports and revision of literature.
Picciolli I et al.
Italian Journal of Pediatrics, 2024
NEXN Gene in Cardiomyopathies and Sudden Cardiac Deaths: Prevalence, Phenotypic Expression, and Prognosis.
Hermida A et al.
Circulation. Genomic and Precision Medicine, 2024
Morphological and genetic causes of fetal cardiomyopathies.
Kohaut E et al.
Clinical Genetics, 2023
Categorized Genetic Analysis in Childhood-Onset Cardiomyopathy.
Al-Hassnan ZN et al.
Circulation. Genomic and Precision Medicine, 2020
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