Genetic workup as a complementary tool for the diagnosis of primary complement component deficiencies: a multicenter experience.

Autor: Shamriz, Oded1,2, Simon, Amos J.3, Frizinsky, Shirley4, Lev, Atar4,5, Megged, Orli6, Barel, Ortal7,8,9, Marcus, Nufar5,7,10, Tal, Yuval1, Somech, Raz4,5, Toker, Ori5,11 oritoker@szmc.org.il
Zdroj: European Journal of Pediatrics. May2022, Vol. 181 Issue 5, p1997-2004. 8p. 2 Diagrams, 2 Charts, 1 Graph.
Databáze: Academic Search Ultimate
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