Pages that link to "Q35607929"
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The following pages link to Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations (Q35607929):
Displaying 42 items.
- Cardiac troponin mutations and restrictive cardiomyopathy (Q21328674) (← links)
- Genetic counselling for hypertrophic cardiomyopathy: are we ready for it? (Q24792466) (← links)
- Clinical utility of cardiovascular magnetic resonance in hypertrophic cardiomyopathy (Q26999424) (← links)
- The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms (Q28203734) (← links)
- Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands (Q28283579) (← links)
- Contractile protein mutations and heart disease (Q28288865) (← links)
- Sudden cardiac death in patients with hypertrophic cardiomyopathy: from bench to bedside with an emphasis on genetic markers (Q33173818) (← links)
- Familial hypertrophic cardiomyopathy owing to double heterozygosity for a 403Arg--> Trp mutation in exon 13 of the MYH7 gene and a novel mutation, 453Arg--> His, in exon 14 of the MYH7 gene: A case report. (Q33807877) (← links)
- Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene (Q33909960) (← links)
- Molecular genetics and pathogenesis of hypertrophic cardiomyopathy (Q34021080) (← links)
- Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy (Q34120159) (← links)
- Differential methylation of CpG sites in two isoforms of myosin binding protein C, an important hypertrophic cardiomyopathy gene. (Q34133294) (← links)
- Structural interpretation of the mutations in the beta-cardiac myosin that have been implicated in familial hypertrophic cardiomyopathy (Q34386835) (← links)
- Modifier genes for hypertrophic cardiomyopathy (Q34641881) (← links)
- Independent origin of identical beta cardiac myosin heavy-chain mutations in hypertrophic cardiomyopathy (Q35195188) (← links)
- Coexistence of mitochondrial DNA and beta myosin heavy chain mutations in hypertrophic cardiomyopathy with late congestive heart failure (Q35369864) (← links)
- Long genes and genes with multiple splice variants are enriched in pathways linked to cancer and other multigenic diseases. (Q35954511) (← links)
- Molecular genetics in hypertrophic cardiomyopathy: towards individualized management of the disease (Q36344118) (← links)
- Angiotensin-converting enzyme and angiotensinogen gene polymorphism in hypertrophic cardiomyopathy (Q37276554) (← links)
- A clinical approach to inherited hypertrophy: the use of family history in diagnosis, risk assessment, and management. (Q37504006) (← links)
- Genetic testing for inherited cardiac disease (Q38125385) (← links)
- Genetic test for dilated and hypertrophic cardiomyopathies: useful or less than useful for patients? (Q38125689) (← links)
- The sarcomeric M-region: a molecular command center for diverse cellular processes (Q38471353) (← links)
- Evolving Approaches to Genetic Evaluation of Specific Cardiomyopathies (Q38608486) (← links)
- Molecular basis of hypertrophic and dilated cardiomyopathy (Q40486857) (← links)
- Pre-participation cardiovascular evaluation for athletic participants to prevent sudden death: Position paper from the EHRA and the EACPR, branches of the ESC. Endorsed by APHRS, HRS, and SOLAECE. (Q40488679) (← links)
- Hereditary dilated cardiomyopathy (Q40499701) (← links)
- Multiple disease genes cause hypertrophic cardiomyopathy (Q40602713) (← links)
- A previously undescribed de novo insertion-deletion mutation in the beta myosin heavy chain gene in a kindred with familial hypertrophic cardiomyopathy (Q41341431) (← links)
- The genetic basis of pediatric cardiovascular disease (Q41415560) (← links)
- Molecular genetics of congestive heart failure. (Q41737493) (← links)
- Contractility parameters of human β-cardiac myosin with the hypertrophic cardiomyopathy mutation R403Q show loss of motor function. (Q42119619) (← links)
- A novel Myosin essential light chain mutation causes hypertrophic cardiomyopathy with late onset and low expressivity (Q42173357) (← links)
- When signalling goes wrong: pathogenic variants in structural and signalling proteins causing cardiomyopathies (Q47104776) (← links)
- The cardiac beta-myosin heavy chain gene is not the predominant gene for hypertrophic cardiomyopathy in the Finnish population. (Q52906642) (← links)
- Whole blood RNA offers a rapid, comprehensive approach to genetic diagnosis of cardiovascular diseases. (Q54562154) (← links)
- A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3. (Q55065766) (← links)
- Pre-participation cardiovascular evaluation for athletic participants to prevent sudden death: Position paper from the EHRA and the EACPR, branches of the ESC. Endorsed by APHRS, HRS, and SOLAECE (Q58757143) (← links)
- Familial dilated cardiomyopathy (Q59461183) (← links)
- [Genetic causes of hypertrophic cardiomyopathy] (Q74569442) (← links)
- Analysis of De Novo Mutations in Sporadic Cardiomyopathies Emphasizes Their Clinical Relevance and Points to Novel Candidate Genes (Q89511419) (← links)
- Exploring the Continuum of Hypertrophic Cardiomyopathy-From DNA to Clinical Expression (Q92991260) (← links)