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- [6] Case reports of a c.475G>T, p.E159* lamin A/C mutation with a family history of conduction disorder, dilated cardiomyopathy and sudden cardiac death BMC Cardiovascular Disorders, 19
- [9] Mutation in TNNI3(c. 544G>A): a novel likely pathogenic mechanism of neonatal dilated cardiomyopathy FRONTIERS IN PEDIATRICS, 2023, 11