88 MATERNAL PKU SYNDROME IN COUSINS CAUSED BY MILD, UNRECOGNIZED PHENYLKETONURIA IN THEIR MOTHERS HOMOZYGOUS FOR THE PHENYLALANINE HYDROXYLASE 261 ARG – GLN MUTATION | Zendy

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88 MATERNAL PKU SYNDROME IN COUSINS CAUSED BY MILD, UNRECOGNIZED PHENYLKETONURIA IN THEIR MOTHERS HOMOZYGOUS FOR THE PHENYLALANINE HYDROXYLASE 261 ARG – GLN MUTATION

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