Analysis of NPHS1, NPHS2, ACTN4, and WT1 in Japanese patients with congenital nephrotic syndrome-Reference-Cited by-同舟云学术

Analysis of NPHS1, NPHS2, ACTN4, and WT1 in Japanese patients with congenital nephrotic syndrome

Published:2005-04 Issue:4 Volume:67 Page:1248-1255
ISSN:0085-2538
Container-title:Kidney International
language:en
Short-container-title:Kidney International

Author:

Sako Mayumi,Nakanishi Koichi,Obana Mina,Yata Nahoko,Hoshii Sakurako,Takahashi Shori,Wada Naohiro,Takahashi Yasuhiko,Kaku Yoshitsugu,Satomura Kenichi,Ikeda Masahiro,Honda Masataka,Iijima Kazumoto,Yoshikawa Norishige

Publisher

Elsevier BV

Subject

Nephrology

Reference30 articles.

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5. Structure of the gene for congenital nephrotic syndrome of the Finnish type (NPHS1) and characterization of mutations;Lenkkeri;Am J Hum Genet,1999

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