[MAOB: a modifier gene in phenylketonuria?].

Abstract

Phenylketonuria (PKU), the most frequent inborn error of metabolism (1/15,000 live births), is an autosomal recessive condition caused by phenylalanine hydroxylase deficiency. Despite early and strict dietary control, some PKU children still exhibit behavioral and cognitive difficulties suggestive of a partly prenatal brain injury. The reported variability… (More)

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Cite this paper

@article{Ghozlan2004MAOBAM, title={[MAOB: a modifier gene in phenylketonuria?].}, author={Aline Ghozlan and Arnold Munnich}, journal={Medecine sciences : M/S}, year={2004}, volume={20 10}, pages={929-32} }