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[In addition, a mouse genetics approach has also been used to investigate the disease pathogenesis of Loeys-Dietz syndrome, a familial autosomal dominant human disorder characterized by a dilated aortic root, and associated with mutations in the two TGF? signaling receptor genes, TGFBR1 and TGFBR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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