Understanding the Pathogenesis of Ehlers-Danlos Syndrome, a Rare Connective Tissue Disorder Caused by B3GALT6 Mutations: What if 'Omics' Could Help? - Université de Lorraine Access content directly
Conference Papers Year : 2018

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

C. Bui
Ingénierie Moléculaire et Physiopathologie Articulaire

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Biochemistry, Molecular Biology Human health and pathology

Sandrine Gulberti  : Connect in order to contact the contributor

https://hal.univ-lorraine.fr/hal-02945363

Submitted on : Tuesday, September 22, 2020-11:21:17 AM

Last modification on : Tuesday, June 25, 2024-10:07:21 AM

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hal-02945363 , version 1 (22-09-2020)

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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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