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    • Characterization of the mouse phenylalanine hydroxylase mutation Pah(enu3) 

      Haefele, Mark J.; White, Gabriele; McDonald, J. David (Academic Press, 2001-01)
      Phenylketonuria (PKU) is an inborn error of metabolism that is inherited in an autosomal recessive manner. It arises from a deficiency of phenylalanine hydroxylase, which is responsible for converting phenylalanine to ...