Exome sequencing identifies SMAD3 mutations as a cause of familial thoracic aortic aneurysm and dissection with intracranial and other arterial aneurysms.

Source:http://linkedlifedata.com/resource/pubmed/id/21778426

Circ. Res. 2011 Sep 2 109 6 680-6

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PMID
21778426