A novel homozygous mutation in recombination activating gene 2 in 2 relatives with different clinical phenotypes: Omenn syndrome and hyper-IgM syndrome
Chou, Janet, Hanna-Wakim, Rima, Tirosh, Irit, Kane, Jennifer, Fraulino, David, Lee, Yu Nee, Ghanem, Soha, Mahfouz, Iman, Mégarbané, André, Lefranc, Gérard, Inati, Adlette, Dbaibo, Ghassan, Giliani, SiVolume:
130
Language:
english
Journal:
Journal of Allergy and Clinical Immunology
DOI:
10.1016/j.jaci.2012.06.012
Date:
December, 2012
File:
PDF, 132 KB
english, 2012