Abnormal von Willebrand Factor Multimer Pattern Without VWF Variants in Autosomal-Recessive Cutis Laxa Type IIA Open Access

Funding: This work was supported by award HL140025 the National Heart, Lung, and Blood Institute of the National Institutes of Health, and by the Ernest W. Goodpasture Chair in Experimental Pathology for Translational Research from Vanderbilt University.

Disclosures: None of the authors have conflicts of interest related to this manuscript. Unrelated, D.G. is a consultant for several pharmaceutical companies with interests in developing drugs that target factor XI and prekallikrein.

Data Sharing Statement: All new data generated are available in the article.