Hereditary C1q deficiency and secondary Sjogren's syndrome.

Translated title of the contribution: Hereditary C1q deficiency and secondary Sjogren's syndrome.

E.P.A.H. Hoppenreijs, P. van Dijken, P.J. Kabel, J.M.Th. Draaisma

Research output: Contribution to journal › Article › Academic › peer-review

Translated title of the contribution	Hereditary C1q deficiency and secondary Sjogren's syndrome.
Original language	Undefined/Unknown
Pages (from-to)	1524-1525
Number of pages	2
Journal	Annals of the Rheumatic Diseases
Volume	63
Issue number	11
Publication status	Published - 2004

Cite this

@article{db709ca9b09e4e0a8da11170723355bb,

title = "Hereditary C1q deficiency and secondary Sjogren's syndrome.",

author = "E.P.A.H. Hoppenreijs and {van Dijken}, P. and P.J. Kabel and J.M.Th. Draaisma",

year = "2004",

language = "Undefined/Unknown",

volume = "63",

pages = "1524--1525",

journal = "Annals of the Rheumatic Diseases",

issn = "0003-4967",

publisher = "Elsevier",

number = "11",

}