Understanding the Pathogenesis of Ehlers-Danlos Syndrome, a Rare Connective Tissue Disorder Caused by B3GALT6 Mutations: What if 'Omics' Could Help?

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https://hal.univ-lorraine.fr/hal-01890495
Contributor : Sandrine Gulberti <>
Submitted on : Monday, October 8, 2018 - 4:29:43 PM
Last modification on : Tuesday, October 9, 2018 - 1:15:27 AM

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C. Bui. Understanding the Pathogenesis of Ehlers-Danlos Syndrome, a Rare Connective Tissue Disorder Caused by B3GALT6 Mutations: What if 'Omics' Could Help?. Proteoglycans Gordon Research Conference, Proteoglycans in Homeostasis and Disease: Cracking the PG Code, Jul 2018, Andover, NH, United States. ⟨hal-01890495⟩

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