These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

207 related items for PubMed ID: 23159873

  • 1. A new ATP7B gene mutation with severe condition in two unrelated Iranian families with Wilson disease.
    Dastsooz H, Dehghani SM, Imanieh MH, Haghighat M, Moini M, Fardaei M.
    Gene; 2013 Feb 01; 514(1):48-53. PubMed ID: 23159873
    [Abstract] [Full Text] [Related]

  • 2. Mutation analysis of ATP7B gene in Turkish Wilson disease patients: identification of five novel mutations.
    Simsek Papur O, Akman SA, Cakmur R, Terzioglu O.
    Eur J Med Genet; 2013 Apr 01; 56(4):175-9. PubMed ID: 23333878
    [Abstract] [Full Text] [Related]

  • 3. Spectrum of mutations in the ATP binding domain of ATP7B gene of Wilson Disease in a regional Indian cohort.
    Guggilla SR, Senagari JR, Rao PN, Madireddi S.
    Gene; 2015 Sep 10; 569(1):83-7. PubMed ID: 25982861
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Analysis of exon 8 of ATP7B gene in Thai patients with Wilson disease.
    Keandaungjuntr J, Busabaratana M, Kositchaiwat C, Sura T, Pulkes T.
    J Med Assoc Thai; 2011 Oct 10; 94(10):1184-8. PubMed ID: 22145502
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Mutations of ATP7B gene in Wilson disease in Japan: identification of nine mutations and lack of clear founder effect in a Japanese population.
    Yamaguchi A, Matsuura A, Arashima S, Kikuchi Y, Kikuchi K.
    Hum Mutat; 1998 Oct 10; Suppl 1():S320-2. PubMed ID: 9452121
    [No Abstract] [Full Text] [Related]

  • 10. Mutation analysis of the ATP7B gene and genotype-phenotype correlation in Chinese patients with Wilson disease.
    Li M, Ma J, Wang W, Yang X, Luo K.
    BMC Gastroenterol; 2021 Sep 01; 21(1):339. PubMed ID: 34470610
    [Abstract] [Full Text] [Related]

  • 11. Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses.
    Shah AB, Chernov I, Zhang HT, Ross BM, Das K, Lutsenko S, Parano E, Pavone L, Evgrafov O, Ivanova-Smolenskaya IA, Annerén G, Westermark K, Urrutia FH, Penchaszadeh GK, Sternlieb I, Scheinberg IH, Gilliam TC, Petrukhin K.
    Am J Hum Genet; 1997 Aug 01; 61(2):317-28. PubMed ID: 9311736
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Molecular pathogenesis of Wilson disease among Indians: a perspective on mutation spectrum in ATP7B gene, prevalent defects, clinical heterogeneity and implication towards diagnosis.
    Gupta A, Chattopadhyay I, Dey S, Nasipuri P, Das SK, Gangopadhyay PK, Ray K.
    Cell Mol Neurobiol; 2007 Dec 01; 27(8):1023-33. PubMed ID: 17823867
    [Abstract] [Full Text] [Related]

  • 18. Gene symbol: ATP7B. Disease: Wilson disease.
    Ray K, Gupta A.
    Hum Genet; 2008 Oct 01; 124(3):297. PubMed ID: 18846616
    [No Abstract] [Full Text] [Related]

  • 19. Mutational characterization of ATP7B gene in 103 Wilson's disease patients from Southern China: identification of three novel mutations.
    Wei Z, Huang Y, Liu A, Diao S, Yu Q, Peng Z, Hong M.
    Neuroreport; 2014 Oct 01; 25(14):1075-80. PubMed ID: 25089800
    [Abstract] [Full Text] [Related]

  • 20. [Genotype and phenotype correlation in Chinese patients with Wilson's Disease].
    Liu XQ, Zhang YF, Liu TT, Gu XF, Hsiao KJ, Bao KR, Yu LH.
    Zhonghua Er Ke Za Zhi; 2003 Jan 01; 41(1):35-8. PubMed ID: 14761325
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.