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2011
Mark Molecular basis of hereditary C1q deficiency-revisited: identification of several novel disease-causing mutations
Schejbel, L. ; Melander Skattum, Lillemor ^LU ; Hagelberg, S. ; Ahlin, A. ; Schiller, B. ; Berg, S. ; Genel, F. ; Truedsson, Lennart ^LU and Garred, P. (2011) In Genes and Immunity 12(8). p.626-634
- Contribution to journal › Article
2007
Mark C1q deficiency in an Inuit family: Identification of a new class of C1q disease-causing mutations
Marquart, Hanne Vibeke ; Schejbel, Lone ; Sjöholm, Anders ^LU ; Mårtensson, Ulla ^LU ; Nielsen, Susan ; Koch, Anders ; Svejgaard, Arne and Garred, Peter (2007) In Clinical Immunology 124(1). p.33-40
- Contribution to journal › Article