The pathogenesis of molybdenum cofactor deficiency, its delay by maternal clearance, and its expression pattern in microarray analysis

Author:

Reiss Jochen,Bonin Michael,Schwegler Herbert,Sass Jörn Oliver,Garattini Enrico,Wagner Silke,Lee Heon-Jin,Engel Wolfgang,Riess Olaf,Schwarz Günter

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference35 articles.

1. The pterin molybdenum cofactors;Rajagopalan;J. Biol. Chem.,1992

2. Mammalian molybdo-flavoenzymes, an expanding family of proteins: structure, genetics, regulation, function and pathophysiology;Garattini;Biochem. J.,2003

3. Molybdenum cofactor deficiency and isolated sulfite oxidase deficiency;Johnson,2001

4. Hereditary xanthinuria;Simmonds,1995

5. Molybdopterin–problems and perspectives;Rajagopalan;Biofactors,1988

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