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 |
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Zdroj: | Human Molecular Genetics; Jul1993, Vol. 2 Issue 7, p1061-1062, 2p |
Databáze: | Complementary Index |
Externí odkaz: |