Mutations in the PAH gene: A Tool for population genetics study

Mutations in the PAH gene: A Tool for population genetics study

Phenylketonuria (PKU), an inborn error of metabolism, is caused by mutations in the phenylalanine hydroxylase (PAH) gene. In the Serbian population, 19 different PAH mutations have been identified. We used PAH mutations as molecular markers for population genetics study. The low homozygosity value o...

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Bibliographic Details
Main Authors: Stojiljković Maja, Stevanović Ana, Đorđević Maja, Petručev Branka, Tošić Nataša, Karan-Đurašević Teodora, Aveić Sanja, Radmilović Milena, Pavlović Sonja
Format: Article
Language:English
Published: University of Belgrade, University of Novi Sad 2007-01-01
Series:Archives of Biological Sciences
Subjects:
Phenylketonuria
phenylalanine hydroxylase gene mutations
homozygosity value
expected heterozygosity
haplotype analysis
Online Access:http://www.doiserbia.nb.rs/img/doi/0354-4664/2007/0354-46640703161S.pdf

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http://www.doiserbia.nb.rs/img/doi/0354-4664/2007/0354-46640703161S.pdf

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