Autosomal dominant tubulointerstitial kidney disease (ADTKD) in Ireland

Introduction: Autosomal dominant tubulointerstitial kidney disease (ADTKD) is a rare genetic cause of renal impairment resulting from mutations in the MUC1, UMOD, HNF1B, REN, and SEC61A1 genes. Neither the national or global prevalence of these diseases has been determined. We aimed to establish a d...

詳細記述

保存先:
書誌詳細
出版年:Ren Fail
主要な著者: Cormican, S., Connaughton, D. M., Kennedy, C., Murray, S., Živná, M., Kmoch, S., Fennelly, N. K., O’Kelly, P., Benson, K. A., Conlon, E. T., Cavalleri, G., Foley, C., Doyle, B., Dorman, A., Little, M. A., Lavin, P., Kidd, K., Bleyer, A. J., Conlon, P. J.
フォーマット: Artigo
言語:Inglês
出版事項: Taylor & Francis 2019
主題:
Clinical Study
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC6746258/
https://ncbi.nlm.nih.gov/pubmed/31509055
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/0886022X.2019.1655452
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