102 related articles for article (PubMed ID: 11775546)
1. Identification of a mutation hotspot in exon 8 of Wilson disease gene by cycle sequencing.
Fan Y; Yu L; Jiang Y; Xu Y; Yang R; Han Y; Cui Y; Ren M; Zhao S
Chin Med J (Engl); 2000 Feb; 113(2):172-4. PubMed ID: 11775546
[TBL] [Abstract][Full Text] [Related]
2. Identification and analysis of mutations of the Wilson disease gene in Chinese population.
Wu Z; Wang N; Murong S; Lin M
Chin Med J (Engl); 2000 Jan; 113(1):40-3. PubMed ID: 11775208
[TBL] [Abstract][Full Text] [Related]
3. Mutation analysis of Taiwanese Wilson disease patients.
Wan L; Tsai CH; Tsai Y; Hsu CM; Lee CC; Tsai FJ
Biochem Biophys Res Commun; 2006 Jun; 345(2):734-8. PubMed ID: 16696937
[TBL] [Abstract][Full Text] [Related]
4. [Identification of a mutation hotspot in exon 8 of Wilson's disease gene by cycle sequencing].
Xu Y; Fan Y; Yu L; Jiang Y; Yang R; Han Y; Cui Y; Ren M; Zhao S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Oct; 15(5):284-7. PubMed ID: 9758874
[TBL] [Abstract][Full Text] [Related]
5. Three novel mutations (P760L, L1305P, Q1351Stop) causing Wilson disease.
Genschel J; Czlonkowska A; Sommer G; Buettner C; Bochow B; Lochs H; Schmidt H
Hum Mutat; 2001 Feb; 17(2):156. PubMed ID: 11180609
[No Abstract] [Full Text] [Related]
6. [Identification of a novel missense mutation in Wilson disease gene].
Yang R; Fan Y; Yu L
Zhonghua Yi Xue Za Zhi; 1997 May; 77(5):344-7. PubMed ID: 9772488
[TBL] [Abstract][Full Text] [Related]
7. [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):91-3. PubMed ID: 10194254
[TBL] [Abstract][Full Text] [Related]
8. Efficient detection of mutations in Wilson disease by manifold sequencing.
Waldenström E; Lagerkvist A; Dahlman T; Westermark K; Landegren U
Genomics; 1996 Nov; 37(3):303-9. PubMed ID: 8938442
[TBL] [Abstract][Full Text] [Related]
9. Mutation analysis in patients with Wilson disease: identification of 4 novel mutations. Mutation in brief no. 250. Online.
Haas R; Gutierrez-Rivero B; Knoche J; Böker K; Manns MP; Schmidt HH
Hum Mutat; 1999; 14(1):88. PubMed ID: 10447265
[TBL] [Abstract][Full Text] [Related]
10. Identification of a novel missense mutation in Wilson's disease gene.
Fan Y; Yang R; Yu L; Wu M; Shi S; Ren M; Han Y; Hu J; Zhao S
Chin Med J (Engl); 1997 Nov; 110(11):887-90. PubMed ID: 9772425
[TBL] [Abstract][Full Text] [Related]
11. [Study on mutation of exon 8 of Wilson's disease gene].
Xu P; Liang X; Ma S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Apr; 16(2):88-90. PubMed ID: 10194253
[TBL] [Abstract][Full Text] [Related]
12. A novel RNA splicing mutation in Japanese patients with Wilson disease.
Shimizu N; Kawase C; Nakazono H; Hemmi H; Shimatake H; Aoki T
Biochem Biophys Res Commun; 1995 Dec; 217(1):16-20. PubMed ID: 8526905
[TBL] [Abstract][Full Text] [Related]
13. R778L, H1069Q, and I1102T mutation study in neurologic Wilson disease.
Kalita J; Somarajan BI; Misra UK; Mittal B
Neurol India; 2010; 58(4):627-30. PubMed ID: 20739809
[TBL] [Abstract][Full Text] [Related]
14. New mutation (T1232P) of the ATP-7B gene associated with neurologic and neuropsychiatric dominance onset of Wilson's disease in three unrelated Colombian kindred.
Velez-Pardo C; Rio MJ; Moreno S; Ramírez-Gomez L; Correa G; Lopera F
Neurosci Lett; 2004 Sep; 367(3):360-4. PubMed ID: 15337266
[TBL] [Abstract][Full Text] [Related]
15. [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; 41(1):35-8. PubMed ID: 14761325
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Common mutations of ATP7B in Wilson disease patients from Hungary.
Firneisz G; Lakatos PL; Szalay F; Polli C; Glant TT; Ferenci P
Am J Med Genet; 2002 Feb; 108(1):23-8. PubMed ID: 11857545
[TBL] [Abstract][Full Text] [Related]
18. [Direct sequencing and analysis of exons of Wilson' disease gene with the most mutations: a study in Hunan Han patients].
Luo KZ; Yang X; Tong DJ; He G; Yi LX
Zhonghua Gan Zang Bing Za Zhi; 2006 Dec; 14(12):920-3. PubMed ID: 17196137
[TBL] [Abstract][Full Text] [Related]
19. Mutational analysis of exon 8 and exon 14 of ATP7B gene in Bangladeshi children with Wilson disease.
Tasmeen R; Karim ASMB; Banu LA; Hossain E; Rokunuzzaman M; Majumder W; Alam ST; Rasid R; Benzamin M; Hasan MS
Indian J Gastroenterol; 2022 Oct; 41(5):456-464. PubMed ID: 36308701
[TBL] [Abstract][Full Text] [Related]
20. Early and severe liver disease associated with homozygosity for an exon 7 mutation, G691R, in Wilson's disease.
Barada K; Nemer G; ElHajj II; Touma J; Cortas N; Boustany RM; Usta J
Clin Genet; 2007 Sep; 72(3):264-7. PubMed ID: 17718866
[No Abstract] [Full Text] [Related]
[Next] [New Search]
