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 …
被引用次数：3 相关文章
[PDF] researchgate.net

[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 …
[PDF] academia.edu

[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 …
[PDF] igjournal.ir

[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 …
[PDF] igjournal.ir

[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 …