ロード中...

Establishment of X-linked Alport syndrome model mice with a Col4a5 R471X mutation

Alport syndrome (AS) is an inherited disorder characterized by glomerular basement membrane (GBM) abnormality and development of chronic kidney disease at an early age. The cause of AS is a genetic mutation in type IV collagen, and more than 80% of patients have X-linked AS (XLAS) with mutation in C...

詳細記述

保存先:
書誌詳細
出版年:Biochem Biophys Rep
主要な著者: Hashikami, Kentarou, Asahina, Makoto, Nozu, Kandai, Iijima, Kazumoto, Nagata, Michio, Takeyama, Michiyasu
フォーマット: Artigo
言語:Inglês
出版事項: Elsevier 2018
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC6295608/
https://ncbi.nlm.nih.gov/pubmed/30582011
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbrep.2018.12.003
タグ: タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!