PKU dietary handbook to accompany PKU guidelines | Orphanet Journal of Rare Diseases | Full Text

PKU dietary handbook to accompany PKU guidelines | Orphanet Journal of Rare Diseases | Full Text

PKU dietary handbook to accompany PKU guidelines

Phenylketonuria (PKU) is an autosomal recessive inborn error of phenylalanine metabolism caused by deficiency in the enzyme phenylalanine hydroxylase that converts phenylalanine into tyrosine.

Authors:A. MacDonald, A. M. J. van Wegberg, K. Ahring, S. Beblo, A. Bélanger-Quintana, A. Burlina, J. Campistol, T. Coşkun, F. Feillet, M. Giżewska, S. C. Huijbregts, V. Leuzzi, F. Maillot, A. C. Muntau, J. C. Rocha, C. Romani…

Citation:Orphanet Journal of Rare Diseases 2020 15:171

Content type:Review

 

Published on: 30 June 2020

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