Literature DB >> 22763404

Mutation spectrum of the PAH gene in the PKU patients from Khorasan Razavi province of Iran.

T Hamzehloei1, S A Hosseini, R Vakili, M Mojarad.   

Abstract

BACKGROUND: Characterization of the molecular basis of phenylketonuria (PKU) in North-east of Iran has been accomplished through the analysis of 62 unrelated chromosomes from 31 Iranian PKU patients.
METHODS: Phenylalanine hydroxylase (PAH) gene mutations have been analyzed by direct DNA sequencing exons 6, 7, 10 and 11.
RESULTS: A mutation detection rate of 74% was achieved. Eleven different mutations were found, with the most frequent mutation, IVS10-11G>A, accounting for 19% of Khorasan-Razavi PKU alleles. Ten mutations (R176X, E280K, IVS11+1G>C, S231P, Q383X, R243X, I224T, E390G, R252W and P281L) represent the rest PKU chromosomes. One novel mutation, Q383X in the homozygote form was identified which is located in the catalytic domain (residues143-410).
CONCLUSION: With this high detection rate of mutations in North-east of Iran, new strategy for carrier testing could be DNA sequencing of these four exons. The other exons and boundaries will be studied only when either one or no mutations are detected in the initial screen.
Copyright © 2012 Elsevier B.V. All rights reserved.

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Year:  2012        PMID: 22763404     DOI: 10.1016/j.gene.2012.06.043

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  8 in total

1.  A novel compound-primed multiplex ARMS-PCR (CPMAP) for simultaneous detection of common PAH gene mutations.

Authors:  Maryam Shaykholeslam Esfahani; Ehsan Shaykholeslam Esfahani; Sadeq Vallian
Journal:  Metab Brain Dis       Date:  2018-04-03       Impact factor: 3.584

2.  Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population.

Authors:  Tina Shirzadeh; Amir Hossein Saeidian; Hamideh Bagherian; Shadab Salehpour; Aria Setoodeh; Mohammad Reza Alaei; Leila Youssefian; Ashraf Samavat; Andrew Touati; Mohammad-Sadegh Fallah; Hassan Vahidnezhad; Morteza Karimipoor; Sarah Azadmehr; Marzieh Raeisi; Ameneh Bandehi Sarhadi; Fatemeh Zafarghandi Motlagh; Mojdeh Jamali; Zahra Zeinali; Maryam Abiri; Sirous Zeinali
Journal:  J Inherit Metab Dis       Date:  2018-08-29       Impact factor: 4.982

3.  Mutation analysis of PAH gene in patients with PKU in western Iran and its association with polymorphisms: identification of four novel mutations.

Authors:  Reza Alibakhshi; Keyvan Moradi; Zahra Mohebbi; Keyghobad Ghadiri
Journal:  Metab Brain Dis       Date:  2013-09-19       Impact factor: 3.584

4.  Spectrum of PAH gene mutations in 1547 phenylketonuria patients from Iran: a comprehensive systematic review.

Authors:  Reza Alibakhshi; Aboozar Mohammadi; Nader Salari; Sahand Khamooshian; Mohsen Kazeminia; Keivan Moradi
Journal:  Metab Brain Dis       Date:  2021-02-24       Impact factor: 3.584

5.  Phenylketonuria in Portugal: Genotype-phenotype correlations using molecular, biochemical, and haplotypic analyses.

Authors:  Filipa Ferreira; Luísa Azevedo; Raquel Neiva; Carmen Sousa; Helena Fonseca; Ana Marcão; Hugo Rocha; Célia Carmona; Sónia Ramos; Anabela Bandeira; Esmeralda Martins; Teresa Campos; Esmeralda Rodrigues; Paula Garcia; Luísa Diogo; Ana Cristina Ferreira; Silvia Sequeira; Francisco Silva; Luísa Rodrigues; Ana Gaspar; Patrícia Janeiro; António Amorim; Laura Vilarinho
Journal:  Mol Genet Genomic Med       Date:  2021-01-19       Impact factor: 2.183

6.  Mutation analysis of Phenylalanine hydroxylase gene in Iranian patients with Phenylketonuria.

Authors:  Mahsa Rastegar Moghadam; Azadeh Shojaei; Vahid Babaei; Farzaneh Rohani; Farideh Ghazi
Journal:  Med J Islam Repub Iran       Date:  2018-03-11

7.  Mutations of the phenylalanine hydroxylase gene in Iranian patients with phenylketonuria.

Authors:  Alireza Biglari; Fatemeh Saffari; Zahra Rashvand; Safarali Alizadeh; Reza Najafipour; Mehdi Sahmani
Journal:  Springerplus       Date:  2015-09-23

8.  Spectrum of Phenylalanine Hydroxylase Gene Mutations in Hamadan and Lorestan Provinces of Iran and Their Associations with Variable Number of Tandem Repeat Alleles.

Authors:  Reza Alibakhshi; Keivan Moradi; Mostafa Biglari; Samaneh Shafieenia
Journal:  Iran J Med Sci       Date:  2018-05
  8 in total

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