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1 Ergebnisse
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Human laminin β2 deficiency causes congenital nephrosis wit..:
Zenker, Martin
;
Aigner, Thomas
;
Wendler, Olaf
...
Human Molecular Genetics. 13 (2004) 21 - p. 2625-2632 , 2004
Link:
https://doi.org/10.1093/hmg/ddh284
RT Journal T1
Human laminin β2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities
UL https://suche.suub.uni-bremen.de/peid=cr-10.1093_hmg_ddh284&Exemplar=1&LAN=DE A1 Zenker, Martin A1 Aigner, Thomas A1 Wendler, Olaf A1 Tralau, Tim A1 Müntefering, Horst A1 Fenski, Regina A1 Pitz, Susanne A1 Schumacher, Valérie A1 Royer-Pokora, Brigitte A1 Wühl, Elke A1 Cochat, Pierre A1 Bouvier, Raymonde A1 Kraus, Cornelia A1 Mark, Karlheinz A1 Madlon, Henry A1 Dötsch, Jörg A1 Rascher, Wolfgang A1 Maruniak-Chudek, Iwona A1 Lennert, Thomas A1 Neumann, Luitgard M. A1 Reis, André PB Oxford University Press (OUP) YR 2004 SN 1460-2083 SN 0964-6906 JF Human Molecular Genetics VO 13 IS 21 SP 2625 OP 2632 LK http://dx.doi.org/https://doi.org/10.1093/hmg/ddh284 DO https://doi.org/10.1093/hmg/ddh284 SF ELIB - SuUB Bremen
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