Different unequal cross-over events between NCF1 and its pseudogenes in autosomal p47phox-deficient chronic granulomatous disease
Author:
Funder
EURO-CGD
European Union
Publisher
Elsevier BV
Subject
Molecular Biology,Molecular Medicine
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4. A p47-phox pseudogene carries the most common mutation causing p47-phox deficient chronic granulomatous disease;Görlach;J. Clin. Invest.,1997
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