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
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?

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hal-02946952 , version 1 (23-09-2020)

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  • HAL Id : hal-02946952 , version 1

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C. Bui, Sandrine Gulberti, Sylvie Fournel-Gigleux. Understanding the Pathogenesis of Ehlers-Danlos Syndrome, a Rare Connective Tissue Disorder Caused by B3GALT6 Mutations: What if 'Omics' Could Help?. 3èmes Journées scientifiques du GDR GAGoSciences, Sep 2018, Lille, France. ⟨hal-02946952⟩
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