Haplotype analysis of phenylalanine hydroxylase alleles in polish families with phenylketonuria.

Abstract:

:Eight polymorphic restriction enzyme sites at phenylalanine hydroxylase locus from the parental chromosomes in Polish families with phenylketonuria were analyzed. Among 28 chromosomes studied, we identified haplotypes found within the Danish population. Haplotype 2 has been found in 25% of affected alleles. One of the patients studied is homozygous for this haplotype.

journal_name

Acta Biochim Pol

journal_title

Acta biochimica Polonica

authors

Jaruzelska J,Borski K,Riess O,Blin N,Słomski R

subject

Has Abstract

pub_date

1989-01-01 00:00:00

pages

323-32

issue

3-4

eissn

0001-527X

issn

1734-154X

journal_volume

36

pub_type

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