How b1,3-Galactosyltransferase 6 defect produces a rare genetic disease, the Ehlers-Danlos syndrome: a functional and molecular investigation - Université de Lorraine Access content directly
Poster Communications Year : 2017

How b1,3-Galactosyltransferase 6 defect produces a rare genetic disease, the Ehlers-Danlos syndrome: a functional and molecular investigation

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hal-01707173 , version 1 (12-02-2018)

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  • HAL Id : hal-01707173 , version 1

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Benjamin Jolivet, Xiaomeng Pang, Fransiska Malfait, Tim Van damme, Sandrine Gulberti, et al.. How b1,3-Galactosyltransferase 6 defect produces a rare genetic disease, the Ehlers-Danlos syndrome: a functional and molecular investigation. 7 Lakes proteoglycans conference: Proteoglycans 2017, Sep 2017, Varese, Italy. ⟨hal-01707173⟩
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