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

Chou J.; Hanna-Wakim R.; Tirosh I.; Kane J.; Fraulino D.; Lee Y.N.; Ghanem S.; Mahfouz I.; Megarbane A.; Lefranc G.; Inati A.; Dbaibo G.; Giliani S.; Notarangelo L.D.; Geha R.S.; Massaad M.J.

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

Chou J.; Hanna-Wakim R.; Tirosh I.; Kane J.; Fraulino D.; Lee Y.N.; Ghanem S.; Mahfouz I.; Megarbane A.; Lefranc G.; Inati A.; Dbaibo G.; Giliani S.; Notarangelo L.D.; Geha R.S.; Massaad M.J.

URI: http://hdl.handle.net/10938/19413

Date: 2012

Abstract:

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

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

Abstract:

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This item appears in the following Collection(s)

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