198 related articles for article (PubMed ID: 15996499)
1. Commentary on Vrabelova et al.
Schmidt HH
Mol Genet Metab; 2005; 86(1-2):11-2. PubMed ID: 15996499
[TBL] [Abstract][Full Text] [Related]
2. Clinical and genetic analysis of pediatric patients with Wilson disease.
Şimşek Papur Ö; Aşık Akman S; Terzioğlu O
Turk J Gastroenterol; 2015 Sep; 26(5):397-403. PubMed ID: 26215059
[TBL] [Abstract][Full Text] [Related]
3. Molecular analysis of Wilson patients: direct sequencing and MLPA analysis in the ATP7B gene and Atox1 and COMMD1 gene analysis.
Bost M; Piguet-Lacroix G; Parant F; Wilson CM
J Trace Elem Med Biol; 2012 Jun; 26(2-3):97-101. PubMed ID: 22677543
[TBL] [Abstract][Full Text] [Related]
4. New mutations and polymorphisms of the ATP7B gene in sporadic Wilson disease.
Lu CX; Qing Lin ; Huang WQ; Tzeng CM
Eur J Med Genet; 2014 Sep; 57(9):498-502. PubMed ID: 24878384
[TBL] [Abstract][Full Text] [Related]
5. Regional distribution of mutations of the ATP7B gene in patients with Wilson disease: impact on genetic testing.
Ferenci P
Hum Genet; 2006 Sep; 120(2):151-9. PubMed ID: 16791614
[TBL] [Abstract][Full Text] [Related]
6. Novel mutations of the ATP7B gene in Han Chinese families with pre-symptomatic Wilson's disease.
Yuan ZF; Wu W; Yu YL; Shen J; Mao SS; Gao F; Xia ZZ
World J Pediatr; 2015 Aug; 11(3):255-60. PubMed ID: 26253413
[TBL] [Abstract][Full Text] [Related]
7. 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; 21(1):339. PubMed ID: 34470610
[TBL] [Abstract][Full Text] [Related]
8. ATP7B mutations in families in a predominantly Southern Indian cohort of Wilson's disease patients.
Santhosh S; Shaji RV; Eapen CE; Jayanthi V; Malathi S; Chandy M; Stanley M; Selvi S; Kurian G; Chandy GM
Indian J Gastroenterol; 2006; 25(6):277-82. PubMed ID: 17264425
[TBL] [Abstract][Full Text] [Related]
9. Genotyping microarray as a novel approach for the detection of ATP7B gene mutations in patients with Wilson disease.
Gojová L; Jansová E; Külm M; Pouchlá S; Kozák L
Clin Genet; 2008 May; 73(5):441-52. PubMed ID: 18371106
[TBL] [Abstract][Full Text] [Related]
10. [Wilson disease: an update].
Seo JK
Korean J Hepatol; 2006 Sep; 12(3):333-63. PubMed ID: 16998287
[TBL] [Abstract][Full Text] [Related]
11. Genetic defects in Indian Wilson disease patients and genotype-phenotype correlation.
Mukherjee S; Dutta S; Majumdar S; Biswas T; Jaiswal P; Sengupta M; Bhattacharya A; Gangopadhyay PK; Bavdekar A; Das SK; Ray K
Parkinsonism Relat Disord; 2014 Jan; 20(1):75-81. PubMed ID: 24094725
[TBL] [Abstract][Full Text] [Related]
12. p.H1069Q mutation in ATP7B and biochemical parameters of copper metabolism and clinical manifestation of Wilson's disease.
Gromadzka G; Schmidt HH; Genschel J; Bochow B; Rodo M; Tarnacka B; Litwin T; Chabik G; Członkowska A
Mov Disord; 2006 Feb; 21(2):245-8. PubMed ID: 16211609
[TBL] [Abstract][Full Text] [Related]
13. 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; 25(14):1075-80. PubMed ID: 25089800
[TBL] [Abstract][Full Text] [Related]
14. Screening for mutations in ATP7B gene using conformation-sensitive gel electrophoresis in a family with Wilson's disease.
Sundaresan S; Eapen CE; Shaji RV; Chandy M; Kurian G; Chandy G
Med Sci Monit; 2007 Mar; 13(3):CS38-40. PubMed ID: 17325640
[TBL] [Abstract][Full Text] [Related]
15. Mutation analysis of the ATP7B gene and genotype/phenotype correlation in 227 patients with Wilson disease.
Vrabelova S; Letocha O; Borsky M; Kozak L
Mol Genet Metab; 2005; 86(1-2):277-85. PubMed ID: 15967699
[TBL] [Abstract][Full Text] [Related]
16. Twenty-four novel mutations in Wilson disease patients of predominantly Italian origin.
Lepori MB; Lovicu M; Dessi V; Zappu A; Incollu S; Zancan L; Giacchino R; Iorio R; Vajro P; Maggiore G; Marcellini M; Barbera C; Pellecchia MT; Simonetti R; Kostic V; Farci AM; Solinas A; De Virgiliis S; Cao A; Loudianos G
Genet Test; 2007; 11(3):328-32. PubMed ID: 17949296
[TBL] [Abstract][Full Text] [Related]
17. Six novel ATP7B mutations in Thai patients with Wilson disease.
Panichareon B; Taweechue K; Thongnoppakhun W; Aksornworanart M; Pithukpakorn M; Yenchitsomanus PT; Limwongse C; Limjindaporn T
Eur J Med Genet; 2011; 54(2):103-7. PubMed ID: 21034864
[TBL] [Abstract][Full Text] [Related]
18. Mutation analysis of Wilson disease in the Spanish population -- identification of a prevalent substitution and eight novel mutations in the ATP7B gene.
Margarit E; Bach V; Gómez D; Bruguera M; Jara P; Queralt R; Ballesta F
Clin Genet; 2005 Jul; 68(1):61-8. PubMed ID: 15952988
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. ATP7B Gene Mutations in Croatian Patients with Wilson Disease.
Ljubić H; Kalauz M; Telarović S; Ferenci P; Ostojić R; Noli MC; Lepori MB; Hrstić I; Vuković J; Premužić M; Radić D; Ravić KG; Sertić J; Merkler A; Barišić AA; Loudianos G; Vucelić B
Genet Test Mol Biomarkers; 2016 Mar; 20(3):112-7. PubMed ID: 26799313
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
