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

By Vazquez N.   Lehrnbecher T.   Chen R.   Christensen B.L.   Gallin J.I.   Malech H.   Holland S.   Zhu S.   Chanock S.J.  

Experimental Hematology, Vol. 29, Iss. 2, 2001-02 ,pp. : 234-243

Elsevier

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Slc19a2: Cloning and Characterization of the Murine Thiamin Transporter cDNA and Genomic Sequence, the Orthologue of the Human TRMA Gene

By Oishi K.   Hirai T.   Gelb B.D.   Diaz G.A.  

Molecular Genetics and Metabolism, Vol. 73, Iss. 2, 2001-06 ,pp. : 149-159

Academic Press

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Gene-scan method for the recognition of carriers and patients with p47 phox -deficient autosomal recessive chronic granulomatous disease

By Dekker J.   de Boer M.   Roos D.  

Experimental Hematology, Vol. 29, Iss. 11, 2001-11 ,pp. : 1319-1325

Elsevier

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Polymorphic Variants in the Human Mitochondrial Cytochrome b Gene

By Andreu A.L.   Bruno C.   Hadjigeorgiou G.M.   Shanske S.   DiMauro S.  

Molecular Genetics and Metabolism, Vol. 67, Iss. 1, 1999-05 ,pp. : 49-52

Academic Press

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Human XPA and XRCC1 DNA Repair Proteins Expressed in Yeast, Saccharomyces cerevisiae

By Pushnova E.A.   Ostanin K.   Thelen M.P.  

Molecular Genetics and Metabolism, Vol. 74, Iss. 3, 2001-11 ,pp. : 380-384

Academic Press

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