A 22-bp deletion in the phenylalanine hydroxylase gene causing phenylketonuria in an Arab family
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference25 articles.
1. A single origin of phenylketonuria in Yemenite Jews
2. A 3-base pair in-frame deletion of the phenylalanine hydroxylase gene results in a kinetic variant of phenylketonuria
3. Phenylketonuria (PKU) in Israel
4. Heterogeneity of phenylketonuria at the clinical, protein and DNA levels
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1. Genetic Disorders Among the Palestinians;Genetic Disorders Among Arab Populations;2010
2. Mutation spectrum and phenylalanine hydroxylase RFLP/VNTR background in 44 Romanian phenylketonuric alleles;Human Mutation;1998
3. Preliminary studies on the molecular basis of hyperphenylalaninemia in Egypt;Human Genetics;1996-05-30
4. 6 Molecular Genetics of Phenylketonuria: From Molecular Anthropology to Gene Therapy;Advances in Genetics;1995
5. Novel frame shift deletions of the phenylalanine hydroxylase gene in phenylketonuria;Human Molecular Genetics;1994
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