Article
The pathogenesis of molybdenum cofactor deficiency, its delay by maternal clearance, and its expression pattern in microarray analysis.
Molecular genetics and metabolism - 1 May 2005
Reiss Jochen, Bonin Michael, Schwegler Herbert, Sass Jörn Oliver, Garattini Enrico, Wagner Silke, Lee Heon-Jin, Engel Wolfgang, Riess Olaf, Schwarz Günter
Abstract excerpt
Molybdenum cofactor (Moco)-deficiency is a lethal autosomal recessive disease, for which until now no effective therapy is available. The biochemical hallmark of this disorder is the inactivity of the Moco-dependent sulfite oxidase, which results in elevated sulfite and diminished sulfate levels throughout the organism. In humans, Moco-deficiency results in neurological damage, which is apparent in untreatable...
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