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256 related items for PubMed ID: 24510568

  • 1. [Mutations of the phenylalanine hydroxylase gene in phenylketonuria patients from Shaanxi].
    Qiang R, Yu W, Cai N, Wang X, Qin C, Zhang L, Ma X, Wang L, Shi X, Liu H, Li X, Wang X, He J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Feb; 31(1):74-7. PubMed ID: 24510568
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  • 2. [Analysis of mutations in exon 7 of phenylalanine hydroxylase gene among children with phenylketonuria in Ningxia, China].
    Mao XM, He J, Liu Y, Li XQ, Yu WZ, Gao ZH, Cai J.
    Zhongguo Dang Dai Er Ke Za Zhi; 2014 Mar; 16(3):259-62. PubMed ID: 24661517
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  • 4. Mutational spectrum of the phenylalanine hydroxylase gene in patients with phenylketonuria in the central region of China.
    Zhang Z, Gao JJ, Feng Y, Zhu LL, Yan H, Shi XF, Chang AM, Shi Y, Wang P.
    Scand J Clin Lab Invest; 2018 May; 78(3):211-218. PubMed ID: 29390883
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  • 14. PAH mutation spectrum and correlation with PKU manifestation in north Jiangsu province population.
    Wang ZW, Jiang SW, Zhou BC.
    Kaohsiung J Med Sci; 2018 Feb; 34(2):89-94. PubMed ID: 29413232
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  • 16. Ten novel mutations in the phenylalanine hydroxylase gene (PAH) observed in Brazilian patients with phenylketonuria.
    Acosta AX, Silva WA, Carvalho TM, Zago MA.
    Hum Mutat; 2001 Feb; 17(1):77. PubMed ID: 11139255
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  • 20. [Identification of novel mutations in the phenylalanine hydroxylase gene of classical phenylketonuria].
    Zhang J, Meng J, Zhai X, Fang G, Gao J, Shi M, Wang Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr; 22(2):134-7. PubMed ID: 15793771
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