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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-02946919
Contributor : Sandrine Gulberti <>
Submitted on : Wednesday, September 23, 2020 - 3:14:50 PM
Last modification on : Tuesday, October 13, 2020 - 10:46:11 AM

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  • HAL Id : hal-02946919, 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-02946919⟩

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