What causes phenylketonuria?

Label:
What causes phenylketonuria?

Description:
The PAH gene produces an enzyme that breaks down the amino acid phenylalanine. Mutations in the PAH gene can cause phenylketonuria (PKU), a disorder that can change cells in the brain. The faulty protein allows dangerously high levels of phenylalanine to accumulate in the brain, poisoning the cells. If a person with PKU consumes too much phenylalanine, the build-up can cause mental retardation.

Biological elements:
chromosome 12

Concepts precesses:

Tools & methods :



Your Genes, Your Health ( YGYH )
DNA From The Beginning ( DNAFTB )
Dolan DNA Learning Center ( DNALC )
Genetic Origins ( GeneticOrigins )
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