The identification of a novel splicing mutation in C1qB in a Japanese family with C1q deficiency: a case report

Complement C1q Activates Canonical Wnt Signaling and Promotes Aging-Related Phenotypes

(2012) Atsuhiko T. Naito et al.   CELL

C1q deficiency: identification of a novel missense mutation and treatment with fresh frozen plasma

(2012) Rezan Topaloglu et al.   CLINICAL RHEUMATOLOGY

Identification of novel coding mutation in C1qA gene in an African–American pedigree with lupus and C1q deficiency

(2012) B Namjou et al.   LUPUS

Molecular basis of hereditary C1q deficiency—revisited: identification of several novel disease-causing mutations

(2011) L Schejbel et al.   GENES AND IMMUNITY

An Infantile Case of Early Manifestation of SLE-like Symptoms in Complete C1q Deficiency

(2011) Jun Hayakawa et al.   JOURNAL OF NIPPON MEDICAL SCHOOL

Impact of C1q deficiency on the severity and outcome of childhood systemic lupus erythematosus

(2010) Sulaiman M. AL-MAYOUF et al.   International Journal of Rheumatic Diseases

C1q Deficiency Leads to the Defective Suppression of IFN-  in Response to Nucleoprotein Containing Immune Complexes

(2010) D. M. Santer et al.   JOURNAL OF IMMUNOLOGY

SLE with C1q deficiency treated with fresh frozen plasma: a 10-year experience

(2009) P. Mehta et al.   RHEUMATOLOGY