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A clinical case of non-compaction cardiomyopathy with concomitant myopathic syndrome and mutations in the LMNA and KCNH2 genes
(БГМУ, 2022)
A clinical case of a patient with non-compaction cardiomyopathy, early development of life-threatening arrhythmias and conduction disorders, myopathic syndrome and mutations in the LMNA and KCNH2 genes is presented. The ...