We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleMolecular basis of hereditary C1q deficiency-revisited: identification of several novel disease-causing mutations.AuthorsSchejbel, L; Skattum, L; Hagelberg, S; Åhlin, A; Schiller, B; Berg, S; Genel, F; Truedsson, L; Garred, PPublicationGenes & Immunity, 2011, Vol 12, Issue 8, p626ISSN1466-4879Publication typearticleDOI10.1038/gene.2011.39