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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-01707177
Contributor : Sandrine Gulberti <>
Submitted on : Monday, February 12, 2018 - 3:47:10 PM
Last modification on : Tuesday, October 13, 2020 - 10:45:34 AM

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  • HAL Id : hal-01707177, 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. Journées scientifiques du GDR GAGoSciences, Oct 2017, Grenoble, France. ⟨hal-01707177⟩

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