133 related articles for article (PubMed ID: 19159593)
1. [Genetic heterogeneity of myosin heavy chain 7 gene G823E mutation in familial hypertrophic cardiomyopathy in Chinese].
Wang H; Zou YB; Song L; Wang JZ; Sun K; Song XD; Zhang CN; Hui RT
Zhonghua Yi Xue Za Zhi; 2008 Dec; 88(44):3120-2. PubMed ID: 19159593
[TBL] [Abstract][Full Text] [Related]
2. [The genotype-phenotype correlation of MYH7 gene G15391A mutation and MYBPC3 gene G12101A mutation in familial hypertrophic cardiomyopathy].
WANG H; ZOU YB; WANG JZ; SONG L; SUN K; SONG XD; WANG XJ; ZHANG CN; HUI RT
Zhonghua Xin Xue Guan Bing Za Zhi; 2008 Dec; 36(12):1059-62. PubMed ID: 19134269
[TBL] [Abstract][Full Text] [Related]
3. [Analysis of MYH7, MYBPC3 and TNNT2 gene mutations in 10 Chinese pedigrees with familial hypertrophic cardiomyopathy and the correlation between genotype and phenotype].
Liu WL; Xie WL; Hu DY; Zhu TG; Li YT; Sun YH; Li CL; Li L; Li TC; Bian H; Tong QG; Yang SN; Fan RY; Cui W
Zhonghua Xin Xue Guan Bing Za Zhi; 2006 Mar; 34(3):202-7. PubMed ID: 16630449
[TBL] [Abstract][Full Text] [Related]
4. [Comparative study of gene mutation between Chinese patients with familial and sporadic hypertrophic cardiomyopathy].
Pan GZ; Liu WL; Hu DY; Xie WL; Zhu TG; Li L; Li CL; Bian H
Zhonghua Yi Xue Za Zhi; 2006 Nov; 86(42):2998-3001. PubMed ID: 17288815
[TBL] [Abstract][Full Text] [Related]
5. Dual LQT1 and HCM phenotypes associated with tetrad heterozygous mutations in KCNQ1, MYH7, MYLK2, and TMEM70 genes in a three-generation Chinese family.
Wang L; Zuo L; Hu J; Shao H; Lei C; Qi W; Liu Y; Miao Y; Ma X; Huang CL; Wang B; Zhou X; Zhang Y; Liu L
Europace; 2016 Apr; 18(4):602-9. PubMed ID: 25825456
[TBL] [Abstract][Full Text] [Related]
6. [The genotype-phenotype correlation of the MYH7 gene c.1273G > a mutation in familial hypertrophic cardiomyopathy].
Wang H; Zou YB; Song L; Wang JZ; Sun K; Song XD; Gao S; Zhang CN; Hui RT
Yi Chuan; 2009 May; 31(5):485-8. PubMed ID: 19586842
[TBL] [Abstract][Full Text] [Related]
7. Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model.
Xia Y; Hu J; Li X; Zheng S; Wang G; Tan S; Zou Z; Ling Q; Yang F; Fan X
J Vis Exp; 2022 Aug; (186):. PubMed ID: 35993750
[TBL] [Abstract][Full Text] [Related]
8. [Screening and analysis of the mutations on beta-myosin heavy chain gene in 3 Chinese families with hypertrophic cardiomyopathy].
Feng XL; Fan XP; Yang ZW; Yang FH
Zhonghua Xin Xue Guan Bing Za Zhi; 2011 Feb; 39(2):110-3. PubMed ID: 21426742
[TBL] [Abstract][Full Text] [Related]
9. [Mutations in beta myosin heavy chain gene: two mutations in Chinese with familial hypertrophic cardiomyopathy and the correlation between the genotype and phenotype].
Xie WL; Liu WL; Hu DY; Cui W; Zhu TG; Li CL; Sun YH; Li L; Li TC; Bian H; Tong QG
Zhonghua Yi Xue Za Zhi; 2004 Oct; 84(19):1610-3. PubMed ID: 15569455
[TBL] [Abstract][Full Text] [Related]
10. [Gene screening and phenotype analysis in a pedigree with familial hypertrophic cardiomyopathy from Yunnan Province].
Pang MJ; Ding XX; Zhang Y; Su WH; Zhang H
Zhonghua Xin Xue Guan Bing Za Zhi; 2018 Nov; 46(11):887-891. PubMed ID: 30462978
[No Abstract] [Full Text] [Related]
11. Asn391Thr Mutation of β-Myosin Heavy Chain in a Hypertrophic Cardiomyopathy Family.
Feng X; He T; Wang JG; Zhao P
Int Heart J; 2018 May; 59(3):596-600. PubMed ID: 29743414
[TBL] [Abstract][Full Text] [Related]
12. Prevalence and Phenotypic Expression of Mutations in the MYH7, MYBPC3 and TNNT2 Genes in Families with Hypertrophic Cardiomyopathy in the South of Brazil: A Cross-Sectional Study.
Mattos BP; Scolari FL; Torres MA; Simon L; Freitas VC; Giugliani R; Matte Ú
Arq Bras Cardiol; 2016 Sep; 107(3):257-265. PubMed ID: 27737317
[TBL] [Abstract][Full Text] [Related]
13. [The Val606Met mutation of human beta myosin heavy chain in a Chinese familial hypertrophic cardiomyopathy family].
Yuan JS; Qiao SB; Wang SX; Teng SY; You SJ; Yang WX; Gao RL; Chen JL; Yang YJ
Zhonghua Xin Xue Guan Bing Za Zhi; 2008 Apr; 36(4):313-6. PubMed ID: 19100006
[TBL] [Abstract][Full Text] [Related]
14. Genetic determinants of clinical phenotype in hypertrophic cardiomyopathy.
Velicki L; Jakovljevic DG; Preveden A; Golubovic M; Bjelobrk M; Ilic A; Stojsic S; Barlocco F; Tafelmeier M; Okwose N; Tesic M; Brennan P; Popovic D; Ristic A; MacGowan GA; Filipovic N; Maier LS; Olivotto I
BMC Cardiovasc Disord; 2020 Dec; 20(1):516. PubMed ID: 33297970
[TBL] [Abstract][Full Text] [Related]
15. Novel deletions in MYH7 and MYBPC3 identified in Indian families with familial hypertrophic cardiomyopathy.
Waldmüller S; Sakthivel S; Saadi AV; Selignow C; Rakesh PG; Golubenko M; Joseph PK; Padmakumar R; Richard P; Schwartz K; Tharakan JM; Rajamanickam C; Vosberg HP
J Mol Cell Cardiol; 2003 Jun; 35(6):623-36. PubMed ID: 12788380
[TBL] [Abstract][Full Text] [Related]
16. [Familiar hypertrophic cardiomyopathy caused by a IVS15-1G > A mutation in cardiac myosin-binding protein C gene].
Zou YB; Wang JZ; Wu GR; Song L; Wang SX; Yu H; Zhang Q; Wang H; Hui RT
Zhonghua Xin Xue Guan Bing Za Zhi; 2006 Aug; 34(8):699-702. PubMed ID: 17081393
[TBL] [Abstract][Full Text] [Related]
17. Long-term outcome of 4 Korean families with hypertrophic cardiomyopathy caused by 4 different mutations.
Choi JO; Yu CW; Chun Nah J; Rang Park J; Lee BS; Jeong Choi Y; Cho BR; Lee SC; Woo Park S; Kimura A; Euy Park J
Clin Cardiol; 2010 Jul; 33(7):430-8. PubMed ID: 20641121
[TBL] [Abstract][Full Text] [Related]
18. [Malignant hypertrophic cardiomyopathy caused by the Arg723Gly mutation in beta-myosin heavy chain gene in a Chinese pedigree].
Zheng DD; Yang JH; Dong NZ; Yang XJ; Song JP; Jiang TB; Cheng XJ; Li HX; Zhou BY; Zhao CM; Jiang WP
Zhonghua Xin Xue Guan Bing Za Zhi; 2006 Mar; 34(3):208-11. PubMed ID: 16630450
[TBL] [Abstract][Full Text] [Related]
19. Clinical features, spectrum of causal genetic mutations and outcome of hypertrophic cardiomyopathy in South Africans.
Ntusi NA; Shaboodien G; Badri M; Gumedze F; Mayosi BM
Cardiovasc J Afr; 2016; 27(3):152-158. PubMed ID: 27841901
[TBL] [Abstract][Full Text] [Related]
20. A molecular screening strategy based on beta-myosin heavy chain, cardiac myosin binding protein C and troponin T genes in Italian patients with hypertrophic cardiomyopathy.
Girolami F; Olivotto I; Passerini I; Zachara E; Nistri S; Re F; Fantini S; Baldini K; Torricelli F; Cecchi F
J Cardiovasc Med (Hagerstown); 2006 Aug; 7(8):601-7. PubMed ID: 16858239
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]