Molecular basis of hereditary C1q deficiency associated with SLE and IgA nephropathy in a Turkish family

Author:

Topaloglu Rezan,Bakkaloglu Aysin,Slingsby Jason H.,Mihatsch Michael J.,Pascual M.,Norsworthy Peter,Morley Bernard J.,Saatci Umit,Schifferli Jurg A.,Walport Mark J.

Publisher

Elsevier BV

Subject

Nephrology

Reference32 articles.

1. A case of selective C1q deficiency;Berkel;Turk J Pediat,1977

2. Component deficiencies 1. The first component: C1q. C1r, C1s;Loos;Progr Allergy,1986

3. Hereditary C1q deficiency and systemic lupus erythematosus;Bowness;Quart J Med,1994

4. J.H. Slingsby, P. Norsworthy, G. Pearce, A.K. Vaishnaw, H. Issler, B.J. Morley, M.J. Walport: Homozygous hereditary C1q deficiency and SLE: A new family and the molecular basis of C1q deficiency in three families. Arthritis Rheum (in press)

5. Assigment of the A chain of C1q (C1QA) to the short arm of chromosome 1;Hedge;Cytogenet Cell Genet,1987

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