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bibliographicCitation Bayat A, Yasmeen S, Lund A, Nielsen JB, Møller LB. Mutational and phenotypical spectrum of phenylalanine hydroxylase deficiency in Denmark. Clin Genet. 2016 Sep;90(3):247–51. doi: 10.1111/cge.12692. PMID: 26542770.
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title Mutational and phenotypical spectrum of phenylalanine hydroxylase deficiency in Denmark
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