Identification of Rare Genetic Variants in Familial Spontaneous Coronary Artery Dissection and Evidence for Shared Biological Pathways.

Turley, Tamiel N; Theis, Jeanne L; Evans, Jared M; Fogarty, Zachary C; Gulati, Rajiv; Hayes, Sharonne N; Tweet, Marysia S; Olson, Timothy M

Turley, Tamiel N; Theis, Jeanne L; Evans, Jared M; Fogarty, Zachary C; Gulati, Rajiv; Hayes, Sharonne N; Tweet, Marysia S; Olson, Timothy M.

Afiliação

Turley TN; Molecular Pharmacology and Experimental Therapeutics Track, Mayo Clinic Graduate School of Biomedical Sciences, Mayo Clinic, Rochester, MN 55905, USA.
Theis JL; Cardiovascular Genetics Research Laboratory, Mayo Clinic, Rochester, MN 55905, USA.
Evans JM; Cardiovascular Genetics Research Laboratory, Mayo Clinic, Rochester, MN 55905, USA.
Fogarty ZC; Department of Quantitative Health Sciences, Division of Computational Biology, Mayo Clinic, Rochester, MN 55905, USA.
Gulati R; Department of Quantitative Health Sciences, Division of Computational Biology, Mayo Clinic, Rochester, MN 55905, USA.
Hayes SN; Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Tweet MS; Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Olson TM; Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN 55905, USA.

J Cardiovasc Dev Dis ; 10(9)2023 Sep 12.

Article em En | MEDLINE | ID: mdl-37754822

Palavras-chave

acute coronary syndrome; co-segregation analysis; collagen genes; myocardial infarction; spontaneous coronary artery dissection; whole-genome sequencing

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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Prognostic_studies Idioma: En Revista: J Cardiovasc Dev Dis Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

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