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- W2419508233 abstract "Upon amplification in vitro of the 12th exon area of the human phenylalanine hydroxylase gene followed by allele-specific hybridisation of the amplification product with synthetic probes and its sequencing by the Maxam-Gilbert method, a C----T transition causing phenylketonuria has been identified in Latvian patients." @default.
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- W2419508233 date "1989-12-01" @default.
- W2419508233 modified "2023-09-23" @default.
- W2419508233 title "Identification of a nature of mutation in the 12th exon of phenylalanine hydroxylase gene in patients with phenylketonuria" @default.
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