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Phenylalanine hydroxylase gene mutation R408W is present on 84% of Estonian phenylketonuria chromosomes.
Lilleväli, H; Ounap, K; Metspalu, A.
Affiliation
  • Lilleväli H; Tartu University Institute of Molecular and Cell Biology, Estonian Biocentre, Estonia.
Eur J Hum Genet ; 4(5): 296-300, 1996.
Article in En | MEDLINE | ID: mdl-8946176
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Database: MEDLINE Main subject: Phenylalanine Hydroxylase / Phenylketonurias / Mutation Type of study: Diagnostic_studies / Observational_studies / Risk_factors_studies Limits: Humans / Newborn Country/Region as subject: Europa Language: En Journal: Eur J Hum Genet Journal subject: GENETICA MEDICA Year: 1996 Type: Article Affiliation country: Estonia
Search on Google
Add to My VHL
Print
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PubMed Links

Database: MEDLINE Main subject: Phenylalanine Hydroxylase / Phenylketonurias / Mutation Type of study: Diagnostic_studies / Observational_studies / Risk_factors_studies Limits: Humans / Newborn Country/Region as subject: Europa Language: En Journal: Eur J Hum Genet Journal subject: GENETICA MEDICA Year: 1996 Type: Article Affiliation country: Estonia