Exome sequencing identifies SMAD3 mutations as a cause of familial thoracic aortic aneurysm and dissection with intracranial and other arterial aneurysms
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| Description | scientific article |
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author: Ellen S Regalado NHLBI GO Exome Sequencing Project Deborah A Nickerson Mark J Rieder Suzanne M. Leal Dianna M Milewicz François P. Bernier Jay Shendure Lorne Clarke |
| Publication date | July 21, 2011 |
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