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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

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Role of HMGB1 in cardiovascular diseases

Wei Li1, Andrew E Sama, Haichao Wang

  • 1Department of Emergency Medicine, North Shore University Hospital, New York University School of Medicine, 350 Community Drive, Manhasset, NY 11030, USA.

Current Opinion in Pharmacology
|February 21, 2006
PubMed

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