Associated Papers
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
Whole-exome sequencing: Clinical characterization of pediatric and adult Italian patients affected by different forms of hereditary cardiovascular diseases.
Lenarduzzi S et al.
Molecular Genetics & Genomic Medicine, 2023
36788754 (PubMed )
Supplement: MGG3-11-e2143-s005.xlsx › Foglio1
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