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Year | Number of Results |
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1995 | 1 |
1997 | 1 |
2000 | 1 |
2002 | 1 |
2024 | 0 |
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Identification of novel mutations and the three most common mutations in the human ATP7B gene of Korean patients with Wilson disease.
Genet Med. 2002 Nov-Dec;4(6 Suppl):43S-48S. doi: 10.1097/00125817-200211001-00009.
Genet Med. 2002.
PMID: 12544487
Free article.
The Wilson disease gene: spectrum of mutations and their consequences.
Thomas GR, Forbes JR, Roberts EA, Walshe JM, Cox DW.
Thomas GR, et al.
Nat Genet. 1995 Feb;9(2):210-7. doi: 10.1038/ng0295-210.
Nat Genet. 1995.
PMID: 7626145
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Mutational analysis of ATP7B and genotype-phenotype correlation in Japanese with Wilson's disease.
Okada T, Shiono Y, Hayashi H, Satoh H, Sawada T, Suzuki A, Takeda Y, Yano M, Michitaka K, Onji M, Mabuchi H.
Okada T, et al.
Hum Mutat. 2000;15(5):454-62. doi: 10.1002/(SICI)1098-1004(200005)15:5<454::AID-HUMU7>3.0.CO;2-J.
Hum Mutat. 2000.
PMID: 10790207
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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.
Shah AB, et al.
Am J Hum Genet. 1997 Aug;61(2):317-28. doi: 10.1086/514864.
Am J Hum Genet. 1997.
PMID: 9311736
Free PMC article.
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