Mutation analysis of phenylketonuria patients from Morocco: High prevalence of mutation G352fsdelG and detection of a novel mutation p.K85X
Keywords: PAH, phenylalanine hydroxylase; PKU, phenylketonuria; MHP, mild hyperphenylalaninemia; DGGE, denaturing gradient gel electrophoresis; MLPA, multiplex ligation probe amplificationPKU; Moroccan; PAH gene; G352fsdelG mutation; p.K85X mutation