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Recurrent macroscopic hematuria in a pediatric patient: is it early to diagnose as having type I hereditary C2 deficiency?
Kisla Ekinci, Rabia Miray, Altun, İbrahim, Bisgin, Atil, Atmis, Bahriye, Altintas, Derya Ufuk, Balcı, SibelJournal:
CEN Case Reports
DOI:
10.1007/s13730-020-00487-5
Date:
May, 2020
File:
PDF, 434 KB
2020