A DEFICIENCY IN COG1 CAUSES A NOVEL CONGENITAL DISORDER OF GLYCOSYLATION TYPE II

G. Matthijs, F. Foulquier, R. Zeevaert, J. Jaeken, D. Quelhas, L. Vilarinho, D. Ungar, M. Krieger, W. Annaert

Research output: Contribution to journal › Special issue › peer-review

Original language	English
Pages (from-to)	202-202
Number of pages	1
Journal	Journal of inherited metabolic disease
Volume	28
Publication status	Published - 2005

Cite this

@article{5e66a195a3884627b8b288cc7c107c70,

title = "A DEFICIENCY IN COG1 CAUSES A NOVEL CONGENITAL DISORDER OF GLYCOSYLATION TYPE II",

author = "G. Matthijs and F. Foulquier and R. Zeevaert and J. Jaeken and D. Quelhas and L. Vilarinho and D. Ungar and M. Krieger and W. Annaert",

year = "2005",

language = "English",

volume = "28",

pages = "202--202",

journal = "Journal of inherited metabolic disease",

issn = "0141-8955",

publisher = "Springer",

}

TY - JOUR

T1 - A DEFICIENCY IN COG1 CAUSES A NOVEL CONGENITAL DISORDER OF GLYCOSYLATION TYPE II

AU - Matthijs, G.

AU - Foulquier, F.

AU - Zeevaert, R.

AU - Jaeken, J.

AU - Quelhas, D.

AU - Vilarinho, L.

AU - Ungar, D.

AU - Krieger, M.

AU - Annaert, W.

PY - 2005

Y1 - 2005

M3 - Special issue

SN - 0141-8955

VL - 28

SP - 202

EP - 202

JO - Journal of inherited metabolic disease

JF - Journal of inherited metabolic disease

ER -