Inherited Metabolic Disorders and the Skin

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Keywords	Aminoacidopathies-phenylketonuria/hyperphenylalaninaemia, Biotinidase deficiency, autosomal recessive rare disease-deficient enzyme activity in serum, Classic PKU, phenylalanine-restricted diet-psychomotor delay prevention, Classification of inborn errors of metabolism, Genetic hyperlipoproteinaemias-lipoprotein structural component defects, Homocystinuria, cystathionine β-synthase (CBS) deficiency-genetic disorder of trans-sulphuration, Inborn errors of metabolism-autosomal recessive disorders, Inherited metabolic disorders-and the skin, Phenylketonuria, genetically determined disease-with autosomal recessive inheritance, Skin symptoms of metabolic diseases-and metabolic disorders
Persistent URL	doi.org/10.1002/9781444345384.ch169, hdl.handle.net/1765/89650
Organisation	Erasmus MC: University Medical Center Rotterdam
Citation APA Style AAA Style APA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	de Klerk, J.B.C, & Oranje, A.P. (2011). Inherited Metabolic Disorders and the Skin. doi:10.1002/9781444345384.ch169

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