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32. Vascular Ehlers–Danlos syndrome patient with a novel COL3A1 gene deletion mutation without alteration in the triple sequence of (Gly‐X‐Y) repeat. Issue 11 (29th August 2020) Authors: Hayashi, Shujiro; Lin, Wu; Hamasaki, Yoichiro; Igawa, Ken Journal: Journal of dermatology Issue: Volume 47:Issue 11(2020) Page Start: e390 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗