102 related articles for article (PubMed ID: 11775546)
21. Analysis of the human homologue of the canine copper toxicosis gene MURR1 in Wilson disease patients.
Stuehler B; Reichert J; Stremmel W; Schaefer M
J Mol Med (Berl); 2004 Sep; 82(9):629-34. PubMed ID: 15205742
[TBL] [Abstract][Full Text] [Related]
22. [Genotype-phenotype correlation of patients with wilson disease in Chinese population].
Wu ZY; Wang N; Lin MT; Fang L; Murong SX
Zhonghua Yi Xue Za Zhi; 2003 Feb; 83(4):309-11. PubMed ID: 12812649
[TBL] [Abstract][Full Text] [Related]
23. Identification of a high frequency of mutation at exon 8 of the ATP7B gene in a Chinese population with Wilson disease by fluorescent PCR.
Xu P; Liang X; Jankovic J; Le W
Arch Neurol; 2001 Nov; 58(11):1879-82. PubMed ID: 11708998
[TBL] [Abstract][Full Text] [Related]
24. 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; 94(10):1184-8. PubMed ID: 22145502
[TBL] [Abstract][Full Text] [Related]
25. High incidence and allelic homogeneity of Wilson disease in 2 isolated populations: a prerequisite for efficient disease prevention programs.
Zappu A; Magli O; Lepori MB; Dessì V; Diana S; Incollu S; Kanavakis E; Nicolaidou P; Manolaki N; Fretzayas A; De Virgiliis S; Cao A; Loudianos G
J Pediatr Gastroenterol Nutr; 2008 Sep; 47(3):334-8. PubMed ID: 18728530
[TBL] [Abstract][Full Text] [Related]
26. [Rapid detection of common ATP7B mutations in Wilson disease by high resolution melting analysis].
Zhao X; Liu Y; Huang S; Meng Y; Sun M; Yang W; Zhang X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):515-9. PubMed ID: 18841562
[TBL] [Abstract][Full Text] [Related]
27. Phenotype-genotype correlation in Wilson disease in a large Lebanese family: association of c.2299insC with hepatic and of p. Ala1003Thr with neurologic phenotype.
Usta J; Wehbeh A; Rida K; El-Rifai O; Estiphan TA; Majarian T; Barada K
PLoS One; 2014; 9(11):e109727. PubMed ID: 25390358
[TBL] [Abstract][Full Text] [Related]
28. Homozygous mutations in the conserved ATP hinge region of the Wilson disease gene: association with liver disease.
Barada K; El-Atrache M; El-Hajj II; Rida K; El-Hajjar J; Mahfoud Z; Usta J
J Clin Gastroenterol; 2010 Jul; 44(6):432-9. PubMed ID: 20485189
[TBL] [Abstract][Full Text] [Related]
29. Identification and characterization of a novel splice-site mutation in the Wilson disease gene.
Diao SP; Hong MF; Huang YQ; Wei ZS; Su QX; Peng ZX; Yu QY; Liu AQ; Chen J; Hu L
J Neurol Sci; 2014 Oct; 345(1-2):154-8. PubMed ID: 25086856
[TBL] [Abstract][Full Text] [Related]
30. Wilson disease: high prevalence in a mountainous area of Crete.
Dedoussis GV; Genschel J; Sialvera TE; Bochow B; Manolaki N; Manios Y; Tsafantakis E; Schmidt H
Ann Hum Genet; 2005 May; 69(Pt 3):268-74. PubMed ID: 15845031
[TBL] [Abstract][Full Text] [Related]
31. Gene symbol: ATP7B. Disease: Wilson disease.
Ray K; Gupta A
Hum Genet; 2008 Oct; 124(3):297. PubMed ID: 18846616
[No Abstract] [Full Text] [Related]
32. [Missense mutations of exons 14 and 18 of Wilson's disease gene in Chinese patients].
Wu Z; Wang N; Murong S; Lin M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Apr; 16(2):91-93. PubMed ID: 10200362
[TBL] [Abstract][Full Text] [Related]
33. Mutation analysis of 218 Chinese patients with Wilson disease revealed no correlation between the canine copper toxicosis gene MURR1 and Wilson disease.
Wu ZY; Zhao GX; Chen WJ; Wang N; Wan B; Lin MT; Murong SX; Yu L
J Mol Med (Berl); 2006 May; 84(5):438-42. PubMed ID: 16649058
[TBL] [Abstract][Full Text] [Related]
34. Allele dropout in PCR-based diagnosis of Wilson disease: mechanisms and solutions.
Lam CW; Mak CM
Clin Chem; 2006 Mar; 52(3):517-20. PubMed ID: 16510432
[TBL] [Abstract][Full Text] [Related]
35. [A study of the liver pathology and direct sequencing of all exons of WD gene in a patient with fulminant Wilson disease].
He G; Yang X; Luo KZ; Jiang YF; Chen HC; Lü SW
Zhonghua Gan Zang Bing Za Zhi; 2007 Sep; 15(9):712-3. PubMed ID: 17903386
[No Abstract] [Full Text] [Related]
36. A rare homozygous missense mutation in ATP7B exon 19 in a case of Wilson disease.
Majumdar R; Al-Jumah M; Zaidan R
Eur Neurol; 2004; 51(1):52-4. PubMed ID: 14639035
[No Abstract] [Full Text] [Related]
37. [Analysis of mutations and haplotypes of polymorphic markers in patients with Wilson-Konovalov disease from Bashkir].
Karunas AS; Mersiianova IV; Poliakov AV; Evgrafov OV; Khusnutdinova EK
Genetika; 2000 Jul; 36(7):972-9. PubMed ID: 10994503
[TBL] [Abstract][Full Text] [Related]
38. Strokelike presentation of Wilson disease with homozygosity for a novel T766R mutation.
Pendlebury ST; Rothwell PM; Dalton A; Burton EA
Neurology; 2004 Nov; 63(10):1982-3. PubMed ID: 15557537
[No Abstract] [Full Text] [Related]
39. Genotype-phenotype correlation in Wilson disease.
Horslen S; Hahn SH
J Clin Gastroenterol; 2010 Jul; 44(6):387-8. PubMed ID: 20421802
[No Abstract] [Full Text] [Related]
40. [Another hot point mutation of Wilson disease gene in Chinese: exon 12].
Wu Z; Wang N; Murong S
Zhonghua Yi Xue Za Zhi; 1999 Jun; 79(6):422-4. PubMed ID: 11715435
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
