Deletion in the Cobalamin Synthetase W Domain–Containing Protein 1 Gene Is associated with Congenital Anomalies of the Kidney and Urinary Tract

BACKGROUND: Researchers have identified about 40 genes with mutations that result in the most common cause of CKD in children, congenital anomalies of the kidney and urinary tract (CAKUT), but approximately 85% of patients with CAKUT lack mutations in these genes. The anomalies that comprise CAKUT a...

全面介紹

Na minha lista:
書目詳細資料
發表在:J Am Soc Nephrol
Main Authors: Kanda, Shoichiro, Ohmuraya, Masaki, Akagawa, Hiroyuki, Horita, Shigeru, Yoshida, Yasuhiro, Kaneko, Naoto, Sugawara, Noriko, Ishizuka, Kiyonobu, Miura, Kenichiro, Harita, Yutaka, Yamamoto, Toshiyuki, Oka, Akira, Araki, Kimi, Furukawa, Toru, Hattori, Motoshi
格式: Artigo
語言:Inglês
出版: American Society of Nephrology 2020
主題:
Basic Research
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC6934996/
https://ncbi.nlm.nih.gov/pubmed/31862704
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2019040398
標簽: 添加標簽
沒有標簽, 成為第一個標記此記錄!

相似書籍