Mutational analysis of patients with p47-phox-deficient chronic granulomatous disease: The significance of recombination events between the p47-phox gene (NCF1) and its highly homologous pseudogenes.
Mutational analysis of patients with p47-phox-deficient chronic granulomatous disease: The significance of recombination events between the p47-phox gene (NCF1) and its highly homologous pseudogenes.
复制标题
p47-phox 缺陷型慢性肉芽肿病患者的突变分析：p47-phox 基因 (NCF1) 与其高度同源的假基因之间重组事件的意义。
DOI：
10.1016/s0301-472x(00)00646-9
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发表时间：
2001
影响因子：
2.6
通讯作者：
Chanock,SJ
中科院分区：
文献类型：
--
作者：
Vazquez,N;Lehrnbecher,T;Chen,R;Christensen,BL;Gallin,JI;Malech,H;Holland,S;Zhu,S;Chanock,SJ
