The genetic dysfunction phenylketonuria (PKU) is The lack to metabolize phenylalanine as a result of an absence of the enzyme phenylalanine hydroxylase. Individuals using this dysfunction are generally known as "phenylketonurics" and have to regulate their consumption of phenylalanine. GABA functions just like a “brake” on neuron circuits all through https://federicou073ezt4.mdkblog.com/profile