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Publications by Emily K. Mis
Familial Dilated Cardiomyopathy Associated With a Novel Combination of Compound Heterozygous TNNC1 Variants
Frontiers in Physiology
Physiology
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JAAPA : official journal of the American Academy of Physician Assistants
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A Novel Α-Tropomyosin Mutation (D55N) Associated With Familial Dilated Cardiomyopathy Increases Tropomyosin Binding to Actin
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A Novel Compound Heterozygous Stxbp2 Mutation in a Case With Familial Hemophagocytic Lymphohistiocytosis
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Familial Dilated Cardiomyopathy Caused by a Novel Frameshift in the BAG3 Gene
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Novel Compound Heterozygous TMEM67 Variants in a Vietnamese Family With Joubert Syndrome: A Case Report
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