Understanding the Pathogenesis of Ehlers-Danlos Syndrome, a Rare Connective Tissue Disorder Caused by B3GALT6 Mutations: What if 'Omics' Could Help? - Université de Lorraine
Poster Communications 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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Human health and pathology Genomics [q-bio.GN]

Sandrine Gulberti  : Connect in order to contact the contributor

https://hal.univ-lorraine.fr/hal-02946919

Submitted on : Wednesday, September 23, 2020-3:14:50 PM

Last modification on : Tuesday, June 25, 2024-10:06:50 AM

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hal-02946919 , version 1 (23-09-2020)

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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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