Gastrointestinal manifestations of Iranian patients with LRBA deficiency
J Tafaroji, F Salami, SA Mahdaviani… - … and Genetics Journal, 2018 - igj.tums.ac.ir
Background: Lipopolysaccharide-responsive beige-like anchor protein (LRBA) deficiency is
a rare genetic primary immunodeficiency (PID) disease caused by mutation in the LRBA …
a rare genetic primary immunodeficiency (PID) disease caused by mutation in the LRBA …
[PDF][PDF] Gastrointestinal manifestations of Iranian patients with LRBA deficiency
J Tafaroji, F Salami, SA Mahdaviani, A Shirkani… - researchgate.net
Background: Lipopolysaccharide-responsive beigelike anchor protein (LRBA) deficiency is
a rare genetic primary immunodeficiency (PID) disease caused by mutation in the LRBA …
a rare genetic primary immunodeficiency (PID) disease caused by mutation in the LRBA …
[PDF][PDF] Gastrointestinal manifestations of Iranian patients with LRBA deficiency
J Tafaroji, F Salami, SA Mahdaviani, A Shirkani… - academia.edu
Background: Lipopolysaccharide-responsive beigelike anchor protein (LRBA) deficiency is
a rare genetic primary immunodeficiency (PID) disease caused by mutation in the LRBA …
a rare genetic primary immunodeficiency (PID) disease caused by mutation in the LRBA …
[PDF][PDF] Gastrointestinal manifestations of Iranian patients with LRBA deficiency
J Tafaroji, F Salami, SA Mahdaviani, A Shirkani… - … and Genetics Journal - igjournal.ir
Background: Lipopolysaccharide-responsive beige-like anchor protein (LRBA) deficiency is
a rare genetic primary immunodeficiency (PID) disease caused by mutation in the LRBA …
a rare genetic primary immunodeficiency (PID) disease caused by mutation in the LRBA …
[PDF][PDF] Gastrointestinal manifestations of Iranian patients with LRBA deficiency
J Tafaroji, F Salami, SA Mahdaviani, A Shirkani… - igjournal.ir
Background: Lipopolysaccharide-responsive beigelike anchor protein (LRBA) deficiency is
a rare genetic primary immunodeficiency (PID) disease caused by mutation in the LRBA …
a rare genetic primary immunodeficiency (PID) disease caused by mutation in the LRBA …