(Q43938321)
Statements
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Prenatal diagnosis in two families with autosomal, p47(phox)-deficient chronic granulomatous disease due to a novel point mutation in NCF1. (English)
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Martin de Boer
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Vinita Singh
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Jan Dekker
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Maja Di Rocco
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Dirk Roos
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1 March 2002
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22
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3
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235-240
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Identifiers
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