Autosomal dominant form of type IV collagen nephropathy exists among patients with hereditary nephritis difficult to diagnose clinicopathologically.

Autor: Imafuku, Aya1, Sawa, Naoki1, Hasegawa, Eiko1, Hiramatsu, Rikako1, Kawada, Masahiro1, Hoshino, Junichi1, Tanaka, Kiho1, Ishii, Yasuo1, Takaichi, Kenmei1,2, Ubara, Yoshifumi1,2, Nozu, Kandai3, Iijima, Kazumoto3, Fujii, Takeshi4, Ohashi, Kenichi4,5
Zdroj: Nephrology. Oct2018, Vol. 23 Issue 10, p940-947. 8p.
Databáze: Academic Search Ultimate
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