Identification of XylT1 mutations in Desbusquois dysplasia type 2 and functional consequences on proteoglycan synthesis - Université de Lorraine
Poster Communications Year : 2017

Identification of XylT1 mutations in Desbusquois dysplasia type 2 and functional consequences on proteoglycan synthesis

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Human genetics Subcellular Processes [q-bio.SC]

Sandrine Gulberti  : Connect in order to contact the contributor

https://hal.univ-lorraine.fr/hal-01707720

Submitted on : Tuesday, February 13, 2018-9:38:50 AM

Last modification on : Tuesday, June 25, 2024-10:07:05 AM

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hal-01707720 , version 1 (13-02-2018)

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  • HAL Id : hal-01707720 , version 1

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Catherine Bui, Céline Hubert, Yasemin Alanay, Beyhan Tuysuz, Christine Bole-Feysot, et al.. Identification of XylT1 mutations in Desbusquois dysplasia type 2 and functional consequences on proteoglycan synthesis. LIA-FR3209 “Glycans & Proteoglycans : The Sweet & Smart Molecules of the 21st century”, Oct 2017, Vandoeuvre-les-Nancy, France. ⟨hal-01707720⟩

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