Single Nucleotide Polymorphisms in Coronary Microvascular Dysfunction.
- Resource Type
- Academic Journal
- Authors
- Stein AP; Department of Medicine University of Florida Gainesville FL USA.; Harder J; Department of Medicine University of Florida Gainesville FL USA.; Holmes HR; Department of Medicine University of Florida Gainesville FL USA.; Merz CNB; Barbra Streisand Women's Heart Center Smidt Heart Institute, Cedars-Sinai Medical Center Los Angeles CA USA.; Pepine CJ; Department of Medicine University of Florida Gainesville FL USA.; Division of Cardiovascular Medicine University of Florida Gainesville FL USA.; Keeley EC; Department of Medicine University of Florida Gainesville FL USA.; Division of Cardiovascular Medicine University of Florida Gainesville FL USA.
- Source
- Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 101580524 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2047-9980 (Electronic) Linking ISSN: 20479980 NLM ISO Abbreviation: J Am Heart Assoc Subsets: MEDLINE
- Subject
- Language
- English
Coronary microvascular dysfunction is an underdiagnosed pathologic process that is associated with adverse clinical outcomes. There are data to suggest that coronary microvascular dysfunction, in some cases, may be genetically determined. We present an updated review of single nucleotide polymorphisms in coronary microvascular dysfunction.