Related Articles
Genetic mutation of familial dilated cardiomyopathy based on next‑generation semiconductor sequencing
Whole exome sequencing identified a pathogenic nonsense mutation in LMNA in a family with a progressive cardiac conduction defect: A case report
Role of dystrophin isoforms and associated proteins in muscular dystrophy (review).
TGFBI gene mutations analysis in Chinese families with corneal dystrophies
Compound heterozygous <em>CAPN3</em> variants identified in a family with limb-girdle muscular dystrophy recessive 1