Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations.

Autor: Schumacher V; Max-Planck Institute for Molecular Genetics, Institute of Human Genetics, University of Düsseldorf, Germany., Schärer K, Wühl E, Altrogge H, Bonzel KE, Guschmann M, Neuhaus TJ, Pollastro RM, Kuwertz-Bröking E, Bulla M, Tondera AM, Mundel P, Helmchen U, Waldherr R, Weirich A, Royer-Pokora B

Publikováno v: Kidney international [Kidney Int] 1998 Jun; Vol. 53 (6), pp. 1594-600.