ArticleOrphanet journal of rare diseases2022

Rare and potential pathogenic mutations of LMNA and LAMA4 associated with familial arrhythmogenic right ventricular cardiomyopathy/dysplasia with right ventricular heart failure, cerebral thromboembolism and hereditary electrocardiogram abnormality.

Jia Chen et al.PubMed ↗Full text ↗Publisher ↗

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