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

No file

Dates and versions

hal-01707177 , version 1 (12-02-2018)

Identifiers

  • HAL Id : hal-01707177 , version 1

Cite

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⟩
34 View
0 Download

Share

Gmail Facebook X LinkedIn More