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Journal Abstract Search

349 related items for PubMed ID: 16207219

  • 1. Spectrum of mutations in the Wilson disease gene (ATP7B) in the Bulgarian population.
    Todorov T, Savov A, Jelev H, Panteleeva E, Konstantinova D, Krustev Z, Mihaylova V, Tournev I, Tankova L, Tzolova N, Kremensky I.
    Clin Genet; 2005 Nov; 68(5):474-6. PubMed ID: 16207219
    [No Abstract] [Full Text] [Related]

  • 2. Identification and molecular characterization of 18 novel mutations in the ATP7B gene from Indian Wilson disease patients: genotype.
    Kumar S, Thapa BR, Kaur G, Prasad R.
    Clin Genet; 2005 May; 67(5):443-5. PubMed ID: 15811015
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  • 5. 24 bp deletion and Ala1278 to Val mutation of the ATP7B gene in a Sardinian family with Wilson disease.
    Orrù S, Thomas G, Loizedda A, Cox DW, Contu L.
    Hum Mutat; 1997 May; 10(1):84-5. PubMed ID: 9222767
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  • 10. [Haplotype analysis at R778L mutation of ATP7B gene in Korean patients with Wilson disease].
    Jin HS, Oh B.
    Korean J Hepatol; 2009 Sep; 15(3):295-8. PubMed ID: 19783878
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  • 11. Gene symbol: ATP7B. Disease: Wilson disease.
    Ray K, Gupta A.
    Hum Genet; 2005 Jul; 117(2-3):299. PubMed ID: 16156028
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  • 14. Gene symbol: ATP7B. Disease: Wilson's disease.
    Ray K, Gupta A.
    Hum Genet; 2005 Dec; 118(3-4):541. PubMed ID: 16521267
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  • 15. Gene symbol: ATP7B. Disease: Wilson's Disease.
    Chan P, Yang J.
    Hum Genet; 2005 Dec; 118(3-4):548. PubMed ID: 16521309
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  • 16. Wilson disease.
    Harada M.
    Med Electron Microsc; 2002 Jun; 35(2):61-6. PubMed ID: 12181646
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  • 19. Gene symbol: ATP7B. Disease: Wilson disease.
    Ray K, Gupta A.
    Hum Genet; 2005 Jul; 117(2-3):294. PubMed ID: 16156015
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