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

AIM: Type IV collagen nephropathies include Alport Syndrome and thin basement membrane nephropathy (TBMN), which are caused by mutations in COL4A3/A4/A5 genes. Recently, reports of patients with heterozygous mutations in COL4A3/A4 have been increasing. The clinical course of these patients has a wid...

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Vydáno v:Nephrology (Carlton)
Hlavní autoři: Imafuku, Aya, Nozu, Kandai, Sawa, Naoki, Hasegawa, Eiko, Hiramatsu, Rikako, Kawada, Masahiro, Hoshino, Junichi, Tanaka, Kiho, Ishii, Yasuo, Takaichi, Kenmei, Fujii, Takeshi, Ohashi, Kenichi, Iijima, Kazumoto, Ubara, Yoshifumi
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley & Sons Australia, Ltd 2018
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Original Articles
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6767408/
https://ncbi.nlm.nih.gov/pubmed/28704582
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/nep.13115
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