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Mutations in exon 3 of the PAH gene causing mild hyperphenylalaninemia.
Zekanowski, C; Nowacka, M; Gizewska, M; Filipowicz, J; Cabalska, B; Bal, J.
Affiliation
  • Zekanowski C; Department of Genetics, National Research Institute of Mother and Child, Warszawa, Poland. genmol@imid.med.pl
Genet Test ; 3(3): 297-9, 1999.
Article in En | MEDLINE | ID: mdl-10495930
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Collection: 01-internacional Database: MEDLINE Main subject: Phenylalanine Hydroxylase / Phenylalanine / Phenylketonurias Limits: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Genet Test Journal subject: GENETICA Year: 1999 Document type: Article Affiliation country: Poland Country of publication: United States
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Phenylalanine Hydroxylase / Phenylalanine / Phenylketonurias Limits: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Genet Test Journal subject: GENETICA Year: 1999 Document type: Article Affiliation country: Poland Country of publication: United States