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Phenylalanine hydroxylase deficiency in a population in Germany: mutational profile and nine novel mutations

P Guldberg1, R Mallmann, K F Henriksen

  • 1Danish Center for Human Genome Research, John F. Kennedy Institute, Glostrup, Denmark.

Human Mutation
|January 1, 1996
PubMed
Abstract

No abstract available in PubMed .

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