Defective C3d caused by C3 p.W1034R in inherited atypical hemolytic uremic syndrome.

Autor: Tsuchida, Masafumi1 (AUTHOR), Goto, Shin1 (AUTHOR) gotos@med.niigata‐u.ac.jp, Watanabe, Hirofumi1 (AUTHOR), Goto, Sawako2 (AUTHOR), Yamaguchi, Hiroki1 (AUTHOR), Narita, Ichiei1 (AUTHOR)
Zdroj: Molecular Genetics & Genomic Medicine. Jan2024, Vol. 12 Issue 1, p1-7. 7p.
Databáze: Academic Search Ultimate
Nepřihlášeným uživatelům se plný text nezobrazuje