309 related articles for article (PubMed ID: 31638223)
1. Genetic analysis of monoallelic double MYH7 mutations responsible for familial hypertrophic cardiomyopathy.
Wang B; Wang J; Wang LF; Yang F; Xu L; Li WX; He Y; Zuo L; Yang QL; Shao H; Hu D; Liu LW
Mol Med Rep; 2019 Dec; 20(6):5229-5238. PubMed ID: 31638223
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. A novel mutation of the beta myosin heavy chain gene responsible for familial hypertrophic cardiomyopathy.
Wang J; Xu SJ; Zhou H; Wang LJ; Hu B; Fang F; Zhang XM; Luo YW; He XY; Zhuang SW; Li XM; Liu ZM; Hu DY
Clin Cardiol; 2009 Sep; 32(9):E16-21. PubMed ID: 19645038
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Exome sequencing identifies a novel MYH7 p.G407C mutation responsible for familial hypertrophic cardiomyopathy.
Guo Q; Xu Y; Wang X; Guo Y; Xu R; Sun K; Chen S
DNA Cell Biol; 2014 Oct; 33(10):699-704. PubMed ID: 24963656
[TBL] [Abstract][Full Text] [Related]
6. Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathy.
Blair E; Redwood C; de Jesus Oliveira M; Moolman-Smook JC; Brink P; Corfield VA; Ostman-Smith I; Watkins H
Circ Res; 2002 Feb; 90(3):263-9. PubMed ID: 11861413
[TBL] [Abstract][Full Text] [Related]
7. Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac beta-myosin gene mutations.
Havndrup O; Bundgaard H; Andersen PS; Allan Larsen L; Vuust J; Kjeldsen K; Christiansen M
Cardiovasc Res; 2003 Feb; 57(2):347-57. PubMed ID: 12566107
[TBL] [Abstract][Full Text] [Related]
8. MYH7 Gene-Related Mutation p.V878L Identified in a Chinese Family with Hypertrophic Cardiomyopathy.
Du Y; Wang Y; Han X; Feng Z; Ma A
Int Heart J; 2019 Nov; 60(6):1415-1420. PubMed ID: 31735781
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. [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]
11. [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]
12. Familial hypertrophic cardiomyopathy caused by a de novo Gly716Arg mutation of the β-myosin heavy chain.
Zhao P; Cui HL; He TT; Wang JG; Wang D; Feng XX; Zou YB; Wang YL; Wang JZ; Hui RT; Song L
Cardiol Young; 2017 Apr; 27(3):467-472. PubMed ID: 27161882
[TBL] [Abstract][Full Text] [Related]
13. A low prevalence of MYH7/MYBPC3 mutations among familial hypertrophic cardiomyopathy patients in India.
Bashyam MD; Purushotham G; Chaudhary AK; Rao KM; Acharya V; Mohammad TA; Nagarajaram HA; Hariram V; Narasimhan C
Mol Cell Biochem; 2012 Jan; 360(1-2):373-82. PubMed ID: 21959974
[TBL] [Abstract][Full Text] [Related]
14. [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]
15. Genetics of hypertrophic cardiomyopathy after 20 years: clinical perspectives.
Maron BJ; Maron MS; Semsarian C
J Am Coll Cardiol; 2012 Aug; 60(8):705-15. PubMed ID: 22796258
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [Analysis of genotype and phenotype correlation of MYH7-V878A mutation among ethnic Han Chinese pedigrees affected with hypertrophic cardiomyopathy].
Wang B; Guo R; Zuo L; Shao H; Liu Y; Wang Y; Ju Y; Sun C; Wang L; Zhang Y; Liu L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Aug; 34(4):514-518. PubMed ID: 28777849
[TBL] [Abstract][Full Text] [Related]
18. Identification of novel mutations including a double mutation in patients with inherited cardiomyopathy by a targeted sequencing approach using the Ion Torrent PGM system.
Zhao Y; Cao H; Song Y; Feng Y; Ding X; Pang M; Zhang Y; Zhang H; Ding J; Xia X
Int J Mol Med; 2016 Jun; 37(6):1511-20. PubMed ID: 27082122
[TBL] [Abstract][Full Text] [Related]
19. Lack of Phenotypic Differences by Cardiovascular Magnetic Resonance Imaging in MYH7 (β-Myosin Heavy Chain)- Versus MYBPC3 (Myosin-Binding Protein C)-Related Hypertrophic Cardiomyopathy.
Weissler-Snir A; Hindieh W; Gruner C; Fourey D; Appelbaum E; Rowin E; Care M; Lesser JR; Haas TS; Udelson JE; Manning WJ; Olivotto I; Tomberli B; Maron BJ; Maron MS; Crean AM; Rakowski H; Chan RH
Circ Cardiovasc Imaging; 2017 Feb; 10(2):. PubMed ID: 28193612
[TBL] [Abstract][Full Text] [Related]
20. Investigation of myocardial dysfunction using three-dimensional speckle tracking echocardiography in a genetic positive hypertrophic cardiomyopathy Chinese family.
Wang J; Guo RQ; Guo JY; Zuo L; Lei CH; Shao H; Wang LF; Zhang YM; Liu LW
Cardiol Young; 2018 Sep; 28(9):1106-1114. PubMed ID: 29978770
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
