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

Authors
  • Guldberg, P
  • Lou, H C
  • Henriksen, K F
  • Mikkelsen, I
  • Olsen, B
  • Holck, B
  • Güttler, F
Type
Published Article
Journal
Human Molecular Genetics
Publisher
Oxford University Press (OUP)
Publication Date
Jul 01, 1993
Volume
2
Issue
7
Pages
1061–1062
Identifiers
PMID: 8364546
Source
Medline
License
Unknown
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