A novel missense mutation in the phenylalanine hydroxylase gene of a homozygous Pakistani patient with non-PKU hyperphenylalaninemia.

Autor: Guldberg, Per, C.Lou, Hans, Henriksen, Karen Frils, Mlkkelsen, Ingrld, Olsen, Blrgltte, Hoick, Birgit, Guttler, Flemmlng
Zdroj: Human Molecular Genetics; Jul1993, Vol. 2 Issue 7, p1061-1062, 2p
Databáze: Complementary Index