HAL will be down for maintenance from Friday, June 10 at 4pm through Monday, June 13 at 9am. More information
Skip to Main content Skip to Navigation
Poster communications

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

Complete list of metadata

https://hal.univ-lorraine.fr/hal-01707173
Contributor : Sandrine Gulberti Connect in order to contact the contributor
Submitted on : Monday, February 12, 2018 - 3:44:39 PM
Last modification on : Friday, February 4, 2022 - 3:54:23 PM

Identifiers

  • HAL Id : hal-01707173, version 1

Citation

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⟩

Share

Metrics

Record views

31