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Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 7, p. 3786, doi. 10.3390/ijms22073786
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The Desmin (DES) Mutation p.A337P Is Associated with Left-Ventricular Non-Compaction Cardiomyopathy.
- Published in:
- Genes, 2021, v. 12, n. 1, p. 121, doi. 10.3390/genes12010121
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- Publication type:
- Article