Variants of alpha 1-proteinase inhibitor in black and white South African patients with focal glomerulosclerosis and minimal change nephrotic syndrome.

Author:

Halkas A C,Gaillard M C,Thomson P D,Green S L,Ludewick H,Kala U

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference25 articles.

1. Molecular basis of alpha-l-antitrypsin deficiency;Brantly, M.; Nukiwa, T.; Crystal, R.G.;Am J Med,1988

2. Alpha-iprotease inhibitor in bronchial asthma: phenotypes and biochemical characteristics;Gaillard, M.C.; Kilroe-Smith, T.A.; Nogueira, C.;Am Rev Respir Dis,1992

3. Ethnic differences in the occurrence of the M1 (Ala2'13) haplotype of alpha-lantitrypsin in asthmatic and non-asthmatic black and white South Africans;Gaillard, M.C.; Zwi, S.; Nogueira, C.M.;Clin Genet,1994

4. HLA antigens and atopic features in steroid response nephrotic syndrome of childhood;Thomson, P.D.; Barratt, T.M.; Stokes, C.R.; Turner, M.W.; Soothill, J.F.;Lancet,1976

5. Extracellular matrix remodelling by metalloproteinases and plasminogen activators;Mignatti, P.;Kidney Int,1995

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