Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Disease and meta-analysis and ATP7B[original query] |
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| The H1069Q mutation in ATP7B is associated with late and neurologic presentation in Wilson disease: results of a meta-analysis. Journal of hepatology 2004 Nov 41 (5): 758-63. Stapelbroek Janneke M, Bollen Casper W, van Amstel Johannes K Ploos, van Erpecum Karel J, van Hattum Jan, van den Berg Leonard H, Klomp Leo W J, Houwen Roderick H |
| Homozygosity for Non-H1069Q Missense Mutations in ATP7B Gene and Early Severe Liver Disease: Report of Two Families and a Meta-analysis. JIMD reports 2012 4 129-37. Usta Julnar, Abu Daya Hussein, Halawi Houssam, Al-Shareef Ibraheem, El-Rifai Omar, Malli Ahmad H, Sharara Ala I, Habib Robert H, Barada Kass |
| The global prevalence of Wilson disease from next-generation sequencing data. Genetics in medicine : official journal of the American College of Medical Genetics 2018 Sep . Gao Jiali, Brackley Simon, Mann Jake |
| Copper Imbalance in Alzheimer's Disease: Meta-Analysis of Serum, Plasma, and Brain Specimens, and Replication Study Evaluating ATP7B Gene Variants. Biomolecules 2021 7 11 (7): . Squitti Rosanna, Ventriglia Mariacarla, Simonelli Ilaria, Bonvicini Cristian, Costa Alfredo, Perini Giulia, Binetti Giuliano, Benussi Luisa, Ghidoni Roberta, Koch Giacomo, Borroni Barbara, Albanese Alberto, Sensi Stefano L, Rongioletti Mau |
| A Systematic Review and Meta-Analysis of the R778L Mutation in ATP7B With Wilson Disease in China. Pediatric neurology 2023 6 145 135-147. Ziru Xue, Hongyu Chen, Lan Yu, Peifang Jia |
- Page last reviewed:Feb 1, 2024
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