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 (Q31883583)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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 |
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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 (English)
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Vázquez N
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Lehrnbecher T
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Chen R
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Christensen BL
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Gallin JI
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Malech H
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Holland S
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Zhu S
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Chanock SJ
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1 February 2001
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