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4. Cardiac findings in congenital muscular dystrophies

14. Consensus Statement on Standard of Care for Congenital Muscular Dystrophies

25. Echocardiography

26. Mutations in NEBL encoding the cardiac Z-disk protein nebulette are associated with various cardiomyopathies.

28. Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy.

30. Cardiomyopathy in patients with POMT1-related congenital and limb-girdle muscular dystrophy.

31. Risk of Arrhythmias in MYotonic Dystrophy: trial design of the RAMYD study.

32. Hypertrophic Cardiomyopathy and Primary Restrictive Cardiomyopathy: Similarities, Differences and Phenocopies.

38. MYH7 gene mutation in myosin storage myopathy and scapulo-peroneal myopathy

42. Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy

43. Novel Missense Variant in MYL2 Gene Associated With Hypertrophic Cardiomyopathy Showing High Incidence of Restrictive Physiology.

44. Co-inheritance of mutations associated with arrhythmogenic cardiomyopathy and hypertrophic cardiomyopathy.

45. Consensus statement on standard of care for congenital muscular dystrophies.

46. Risk of arrhythmias in myotonic dystrophy: trial design of the RAMYD study.

47. Generalized lysosome-associated membrane protein-2 defect explains multisystem clinical involvement and allows leukocyte diagnostic screening in Danon disease.

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