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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-02945363
Contributor : Sandrine Gulberti <>
Submitted on : Tuesday, September 22, 2020 - 11:21:17 AM
Last modification on : Tuesday, October 13, 2020 - 10:46:11 AM

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  • HAL Id : hal-02945363, version 1

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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, United States. ⟨hal-02945363⟩

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