Literature DB >> 2337996

Rapid diagnosis of the phenylketonuria haplotype 2 mutation by DNA amplification and MnlI digestion.

H G Eiken1, E Odland, K Hordnes, H Boman, J Apold.   

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Year:  1990        PMID： 2337996

Source DB:  PubMed          Journal:  Clin Chem        ISSN： 0009-9147            Impact factor:   8.327


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  3 in total

1.  Rapid and efficient PCR/StyI test for identification of common mutation R408W in phenylketonuria patients.

Authors:  T Ivaschenko; V S Baranov
Journal:  J Med Genet       Date:  1993-02       Impact factor: 6.318

2.  Haplotype distribution at the phenylalanine hydroxylase locus in PKU families from the Moravian area of Czechoslovakia.

Authors:  L Kozák; D Dvoráková; A Pijácková; J Kamarýt
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

3.  Application of natural and amplification created restriction sites for the diagnosis of PKU mutations.

Authors:  H G Eiken; E Odland; H Boman; L Skjelkvåle; L F Engebretsen; J Apold
Journal:  Nucleic Acids Res       Date:  1991-04-11       Impact factor: 16.971
  3 in total

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