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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Nephrology (Carlton)
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: John Wiley & Sons Australia, Ltd 2018
Matèries:
Original Articles
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars