92 related articles for article (PubMed ID: 9772488)
1. [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]
2. 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]
3. [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]
4. 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]
5. [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]
6. 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]
7. [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]
8. Familial gene analysis for Wilson disease from north-west Indian patients.
Kumar S; Thapa BR; Kaur G; Prasad R
Ann Hum Biol; 2006; 33(2):177-86. PubMed ID: 16684691
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Identification of a novel missense mutation in the cardiac beta-myosin heavy chain gene in a Chinese patient with sporadic hypertrophic cardiomyopathy.
Kuang SQ; Yu JD; Lu L; He LM; Gong LS; Chen SJ; Chen Z
J Mol Cell Cardiol; 1996 Sep; 28(9):1879-83. PubMed ID: 8899546
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. [Novel mutations identified in exon 7 of phenylalanine hydroxylase gene in Chinese].
Sun G; Jiang L; Zhang X; Tong B; Dong G; Sun K
Yi Chuan Xue Bao; 1997; 24(6):492-5. PubMed ID: 9575658
[TBL] [Abstract][Full Text] [Related]
13. [Study of CFTR gene mutation in Chinese CUAVD patients].
Zeng G; Mei H; Zhuang G; Li M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2000 Aug; 17(4):241-3. PubMed ID: 10932005
[TBL] [Abstract][Full Text] [Related]
14. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
15. [Study on mutation of presenilin-1 gene in familial Alzheimer's disease].
Liu XY; Yin LD; Duan Y; Wang YM; Chen BW; Wang Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct; 21(5):455-8. PubMed ID: 15476169
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [A study of PDE6B gene mutation and phenotype in Chinese cases with retinitis pigmentosa].
Cui Y; Zhao KX; Wang L; Wang Q; Zhang W; Chen WY; Wang LM
Zhonghua Yan Ke Za Zhi; 2003 Jan; 39(1):28-32. PubMed ID: 12760810
[TBL] [Abstract][Full Text] [Related]
18. Analysis of ankyrin-B gene mutations in patients with long QT syndrome.
Zhou X; Shimizu M; Konno T; Ino H; Fujino N; Uchiyama K; Mabuchi T; Kaneda T; Fujita T; Masuda E; Kato H; Funada A; Mabuchi H
Nan Fang Yi Ke Da Xue Xue Bao; 2006 Jul; 26(7):901-3, 909. PubMed ID: 16864073
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Molecular analysis of unknown beta-globin gene mutations using polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) technique and its application in Thai families with beta-thalassemias and beta-globin variants.
Chinchang W; Viprakasit V; Pung-Amritt P; Tanphaichitr VS; Yenchitsomanus PT
Clin Biochem; 2005 Nov; 38(11):987-96. PubMed ID: 16139831
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
