How b1,3-Galactosyltransferase 6 defect produces a rare genetic disease, the Ehlers-Danlos syndrome: a functional and molecular investigation - Université de Lorraine
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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Biochemistry, Molecular Biology Human genetics

Sandrine Gulberti  : Connect in order to contact the contributor

https://hal.univ-lorraine.fr/hal-01707170

Submitted on : Monday, February 12, 2018-3:43:25 PM

Last modification on : Tuesday, June 25, 2024-10:07:22 AM

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hal-01707170 , version 1 (12-02-2018)

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  • HAL Id : hal-01707170 , 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. LIA-FR3209 “Glycans & Proteoglycans : The Sweet & Smart Molecules of the 21st century” , Oct 2017, Vandoeuvre-les-Nancy, France. ⟨hal-01707170⟩

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