Defective initiation of glycosaminoglycan synthesis due to B3GALT6 mutations causes a pleiotropic Ehlers-Danlos-syndrome-like connective tissue disorder.
- DOI
- 10.1016/j.ajhg.2013.04.016
- Published
- 2013 Jun 6
- Container
- American journal of human genetics
- Publisher
- Not recorded
- Open access
- yes
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BibTeX
@article{allodium:10.1016/j.ajhg.2013.04.016,
title = {Defective initiation of glycosaminoglycan synthesis due to B3GALT6 mutations causes a pleiotropic Ehlers-Danlos-syndrome-like connective tissue disorder.},
author = {Malfait F and Kariminejad A and Van Damme T and Gauche C and Syx D and Merhi-Soussi F and Gulberti S and Symoens S and Vanhauwaert S and Willaert A and Bozorgmehr B and Kariminejad MH and Ebrahimiadib N and Hausser I and Huysseune A and Fournel-Gigleux S and De Paepe A},
year = {2013},
journal = {American journal of human genetics},
doi = {10.1016/j.ajhg.2013.04.016},
url = {https://doi.org/10.1016/j.ajhg.2013.04.016}
}RIS
TY - JOUR TI - Defective initiation of glycosaminoglycan synthesis due to B3GALT6 mutations causes a pleiotropic Ehlers-Danlos-syndrome-like connective tissue disorder. AU - Malfait F AU - Kariminejad A AU - Van Damme T AU - Gauche C AU - Syx D AU - Merhi-Soussi F AU - Gulberti S AU - Symoens S AU - Vanhauwaert S AU - Willaert A AU - Bozorgmehr B AU - Kariminejad MH AU - Ebrahimiadib N AU - Hausser I AU - Huysseune A AU - Fournel-Gigleux S AU - De Paepe A PY - 2013 JO - American journal of human genetics DO - 10.1016/j.ajhg.2013.04.016 UR - https://doi.org/10.1016/j.ajhg.2013.04.016 ER -
APA
F, M., A, K., T, V. D., C, G., D, S., F, M., S, G., S, S., S, V., A, W., B, B., MH, K., N, E., I, H., A, H., S, F., & A, D. P. (2013). Defective initiation of glycosaminoglycan synthesis due to B3GALT6 mutations causes a pleiotropic Ehlers-Danlos-syndrome-like connective tissue disorder.. American journal of human genetics. https://doi.org/10.1016/j.ajhg.2013.04.016
Source records
- pubmed · retrieved 2026-09-25T17:48:47.730Z