Author:
Zenker Martin,Aigner Thomas,Wendler Olaf,Tralau Tim,Müntefering Horst,Fenski Regina,Pitz Susanne,Schumacher Valérie,Royer-Pokora Brigitte,Wühl Elke,Cochat Pierre,Bouvier Raymonde,Kraus Cornelia,Mark Karlheinz,Madlon Henry,Dötsch Jörg,Rascher Wolfgang,Maruniak-Chudek Iwona,Lennert Thomas,Neumann Luitgard M.,Reis André
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Reference30 articles.
1. Jalanko, H., Kääriäinen, H. and Norio, R. (2002) Nephrotic disorders. In Rimoin, D.L., Connor, J.M., Pyeritz, R.E. and Korf, B.R. (eds), Principles and Practice of Medical Genetics, 4th edn. Churchill Livingstone, London, Vol. 2, pp. 1708–1719.
2. Somlo, S. and Mundel, P. (2000) Getting a foothold in nephrotic syndrome. Nat. Genet., 24, 333–335.
3. Koziell, A., Grech, V., Hussain, S., Lee, G., Lenkkeri, U., Tryggvason, K. and Scambler, P. (2002) Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration. Hum. Mol. Genet., 11, 379–388.
4. Patek, C.E., Fleming, S., Miles, C.G., Bellamy, C.O., Ladomery, M., Spraggon, L., Mullins, J., Hastie, N.D. and Hooper, M.L. (2003) Murine Denys–Drash syndrome: evidence of podocyte de-differentiation and systemic mediation of glomerulosclerosis. Hum. Mol. Genet., 12, 2379–2394.
5. Zenker, M., Tralau, T., Lennert, T., Pitz, S., Mark, K., Madlon, H., Doetsch, J., Reis, A., Müntefering, H. and Neumann, L.M. (2004) Congenital nephrosis, mesangial sclerosis and distinct eye abnormalities with microcoria: an autosomal recessive syndrome. Am. J. Med. Genet., in press.
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