《对“在经临床病理诊断患有常染色体显性遗传性肾小管间质性肾病的患者中检测MUC1变异体”的勘误》，《国际肾脏报告》，第7卷，第4期，2022年4月，第857 - 866页
Corrigendum to "Detecting MUC1 Variants in Patients Clinicopathologically Diagnosed With Having Autosomal Dominant Tubulointerstitial Kidney Disease"Kidney International Reports, Volume 7, Issue 4, April 2022, Pages 857-866.
作者信息
Okada Eri, Morisada Naoya, Horinouchi Tomoko, Fujii Hideki, Tsuji Takayuki, Miura Masayoshi, Katori Hideyuki, Kitagawa Masashi, Morozumi Kunio, Toriyama Takanobu, Nakamura Yuki, Nishikomori Ryuta, Nagai Sadayuki, Kondo Atsushi, Aoto Yuya, Ishiko Shinya, Rossanti Rini, Sakakibara Nana, Nagano China, Yamamura Tomohiko, Ishimori Shingo, Usui Joichi, Yamagata Kunihiro, Iijima Kazumoto, Imasawa Toshiyuki, Nozu Kandai
机构信息
Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Department of Nephrology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
出版信息
Kidney Int Rep. 2023 Mar 13;8(5):1127-1129. doi: 10.1016/j.ekir.2023.02.1090. eCollection 2023 May.
[This corrects the article DOI: 10.1016/j.ekir.2021.12.037.].
[本文更正了文章的数字对象标识符：10.1016/j.ekir.2021.12.037。]
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