Browsing BIO Faculty Scholarship by Subject "Pah gene"

Now showing items 1-1 of 1

A heteroallelic mutant mouse model: A new orthologue for human hyperphenylalaninemia

Sarkissian, Christineh N.; Boulais, D. M.; McDonald, J. David; Scriver, C. R. (Elsevier, 2000-03)

Hyperphenylalaninemias (HPA) are Mendelian disorders resulting from deficiencies in the conversion of phenylalanine to tyrosine. The vast majority are explained by a primary deficiency of phenylalanine hydroxylase (PAH) ...