Phenylketonuria (PKU) TAM NGUYEN CHEM 4700. Introduction PKU is a common inborn metabolic disorder caused by a deficiency of the liver enzyme phenylalanine.
Advances in gene therapy for phenylketonuria (PKU) Cary O. Harding, MD Department of Molecular & Medical Genetics.
Asbjorn F ö lling Lecture “Heroes of PKU—A History”
Advances in gene therapy for phenylketonuria (PKU)
Work done by: Cátia Ferreira (T5) Isa Costa (T6) Jéssica Vasconcelos (T5) Sara Ferreira (T6)
