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

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https://hal.univ-lorraine.fr/hal-01707173
Contributor : Sandrine Gulberti <>
Submitted on : Monday, February 12, 2018 - 3:44:39 PM
Last modification on : Tuesday, October 13, 2020 - 10:45:36 AM

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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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