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Literature summary for 1.14.16.1 extracted from

  • Brenner, E.; Smagulova, F.; Morozov, I.
    Independent origin of rare Y168H mutation of human phenylalanine hydroxylase gene in Russia (2008), Genetika, 44, 1435-1437.
    View publication on PubMed

Protein Variants

Protein Variants Comment Organism
Y168H the mutation is associated with phenylketonuria Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens P00439
-
-

Synonyms

Synonyms Comment Organism
PAH
-
Homo sapiens
phenylalanine hydroxylase
-
Homo sapiens