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...

תיאור מלא

שמור ב:
מידע ביבליוגרפי
הוצא לאור ב: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
פורמט: Artigo
שפה:Inglês
יצא לאור: American Society of Nephrology 2020
נושאים:
Basic Research
גישה מקוונת: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
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