Dru Leistritz

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Purpose:We sought to characterize the natural history of vascular Ehlers–Danlos syndrome in individuals with heterozygous COL3A1 mutations.Methods:We reviewed clinical records for details of vascular, bowel, and organ complications in 1,231 individuals (630 index cases and 601 relatives).Results:Missense and splice-site mutations accounted for more than 90%(More)
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