Аскерова, Т. А.; Ягубова, В. И.; Гусейнова, Ф. Д.; Гасанова, Ш. И.; Велиева, Г. А.
(Ministerul Sănătăţii al Republicii Moldova, Universitatea de Stat de Medicină şi Farmacie “Nicolae Testemiţanu”, 2012)
Phenilketonuria (PKU) – is hereditary disease, with autosome-recessive type of inheritance associated with deficiency of the enzyme phenylalanine
hydroxylas (PheH) necessary for the convertion of phenylalanine to tyrosine. ...