Unusual X-linked SCID phenotype due to mutation of the poly-A addition signal of IL2RG.

被引:0
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作者
Hsu, AP
Tsai, EJ
Anderson, SM
Fischer, RE
Malech, H
Buckley, RH
Puck, JM
机构
[1] NHGRI, Genet & Mol Biol Branch, NIH, Bethesda, MD 20892 USA
[2] Howard Hughes Med Inst, NIH, Res Scholars Program, Coconut Grove, FL 33133 USA
[3] NIAID, Host Def Lab, NIH, Bethesda, MD 20892 USA
[4] Duke Univ, Sch Med, Dept Pediat, Durham, NC 27706 USA
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Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
206
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页码:50 / 50
页数:1
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