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Scriver, C.R., Hurtubise, M., Konecki, D., Phommarinh, M., Prevost, L., Erlandsen, H., Stevens, R., Waters, P.J., Ryan, S., McDonald, D. and Sarkissian, C. (2003) PAHdb 2003: What a locus-specific knowledgebase can do. Hu-man Mutation, 21, 333-334. http://www.pahdb.mcgill. Ca

has been cited by the following article:

• TITLE: PAH mutational spectrum: still expanding

  AUTHORS: Laura Vilarinho, Sofia Esteves, Elisabete Ramos, António Amorim, Luisa Azevedo

  KEYWORDS: Phenylketonuria (PKU); Phenylalanine Hydroxylase; PAH Gene; Novel Mutation

  JOURNAL NAME: Open Journal of Genetics, Vol.1 No.2, September 23, 2011

  ABSTRACT: Phenylketonuria (PKU, MIM 261600) is the most common inborn error of amino acid metabolism. To date, a total of more than 500 mutations have been associated with the disease. In this report, the novel p.Glu182Lys mutation, found in a Portuguese family in combination with the previously reported p.Leu 348Val, is presented and its putative deleterious impact discussed.