Clinical, biomedical , neurological and molecular study of 11 patients with new mutations in PAH gene

PKU is an autosomal recessive disorder. There is a broad spectrum phenotype which depends mainly on residual enzymatic activity and also on other factors such as modifying genes and non-genetic factors. This fact makes us consider that a multidisciplinary study of these patients is necessary to impr...

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Bibliographic Details
Published in:Revista de neurologiá Vol. 31; no. 10; pp. 907 - 910
Main Authors: Mallolas, J, Vilaseca, M A, Campistol, J, Lambruschini, N, Cambra, F J, Fusté, M E, Milà, M
Format: Journal Article
Language:Spanish
Published: Spain 16-11-2000
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