Recurrent spontaneous coronary dissections in a patient with a de novo fibrillin-1 mutation without Marfan syndrome.

Document type:: Case Reports; Letter; Research Support, Non-U.S. Gov't
Author(s):: von Hundelshausen, Philipp; Oexle, Konrad; Bidzhekov, Kiril; Schmitt, Martin M; Hristov, Michael; Blanchet, Xavier; Kaemmerer, Harald; Matyas, Gabor; Meitinger, Thomas; Weber, Christian
Title:: Recurrent spontaneous coronary dissections in a patient with a de novo fibrillin-1 mutation without Marfan syndrome.
Journal title abbreviation:: Thromb Haemost
Year:: 2015
Journal volume:: 113
Journal issue:: 3
Pages contribution:: 668-70
Language:: eng
Fulltext / DOI:: doi:10.1160/TH14-11-0913
Pubmed ID:: http://view.ncbi.nlm.nih.gov/pubmed/25519456
Print-ISSN:: 0340-6245
TUM Institution:: Institut für Humangenetik; Klinik für Kinderkardiologie und angeborene Herzfehler (Prof. Hess)
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