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J. A novel homozygous mutation in recombination activating gene 2 in 2 relatives with different clinical phenotypes: Omenn syndrome and hyper-IgM syndrome

Authors :
Chou, J
Hanna Wakim, R
Tirosh, I
Kane, J
Fraulino, D
Lee, Yn
Ghanem, S
Mahfouz, I
Megarbane, A
Lefranc, G
Inati, A
Dbaibo, G
Giliani, Silvia Clara
Notarangelo, Ld
Geha, Rs
Massaad, M.
Publication Year :
2012

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.od......3662..9c0f2b0fb0d6561daf0e1416ab6d3357

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