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Journal Abstract Search

228 related items for PubMed ID: 30389586

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  • 3. Spectrum of PAH gene mutations in 1547 phenylketonuria patients from Iran: a comprehensive systematic review.
    Alibakhshi R, Mohammadi A, Salari N, Khamooshian S, Kazeminia M, Moradi K.
    Metab Brain Dis; 2021 Jun; 36(5):767-780. PubMed ID: 33625639
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  • 4. Mutation analysis of PAH gene in patients with PKU in western Iran and its association with polymorphisms: identification of four novel mutations.
    Alibakhshi R, Moradi K, Mohebbi Z, Ghadiri K.
    Metab Brain Dis; 2014 Mar; 29(1):131-8. PubMed ID: 24048906
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  • 5. Mutation spectrum of the PAH gene in the PKU patients from Khorasan Razavi province of Iran.
    Hamzehloei T, Hosseini SA, Vakili R, Mojarad M.
    Gene; 2012 Sep 10; 506(1):230-2. PubMed ID: 22763404
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  • 7. Mutations of the phenylalanine hydroxylase gene in Iranian Azeri Turkish patients with phenylketonuria.
    Bonyadi M, Omrani O, Moghanjoghi SM, Shiva S.
    Genet Test Mol Biomarkers; 2010 Apr 10; 14(2):233-5. PubMed ID: 20187763
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  • 11. Mutation Characteristics of Phenylalanine Hydroxylase Gene in Children with Phenylketonuria in Yinchuan City.
    Yu X, Liu F, Wei B, Li M, Lu R, Pan L.
    Discov Med; 2023 Aug 10; 35(177):533-538. PubMed ID: 37553307
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  • 14. Mutational landscape of phenylketonuria in Iran.
    Ajami N, Soleimani A, Jafarzadeh-Esfehani R, Hasanpour M, Rashid Shomali R, Abbaszadegan MR.
    J Cell Mol Med; 2023 Sep 10; 27(17):2457-2466. PubMed ID: 37525467
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  • 16. Mutations of the phenylalanine hydroxylase gene in Iranian patients with phenylketonuria.
    Biglari A, Saffari F, Rashvand Z, Alizadeh S, Najafipour R, Sahmani M.
    Springerplus; 2015 Sep 10; 4():542. PubMed ID: 26413448
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  • 19. [Mutation in the structure of exon 7 of the phenylalanine hydroxylase in phenylketonuria patients from the Novosibirsk area].
    Smagulova FO, Maslennikov AB, Morozov IV, Kitaĭnik GP.
    Genetika; 2000 Jun 10; 36(6):849-52. PubMed ID: 10923269
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