CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
|
0.700 |
CausalMutation
|
CLINVAR |
A low prevalence of sarcomeric gene variants in a Chinese cohort with left ventricular non-compaction.
|
24691700 |
2015 |
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
|
0.700 |
CausalMutation
|
CLINVAR |
Clinical phenotype and outcome of hypertrophic cardiomyopathy associated with thin-filament gene mutations.
|
25524337 |
2014 |
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
|
0.700 |
CausalMutation
|
CLINVAR |
Early results of sarcomeric gene screening from the Egyptian National BA-HCM Program.
|
23233322 |
2013 |
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
|
0.700 |
CausalMutation
|
CLINVAR |
Long-term outcomes in hypertrophic cardiomyopathy caused by mutations in the cardiac troponin T gene.
|
22144547 |
2012 |
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
|
0.700 |
CausalMutation
|
CLINVAR |
IMAGE CARDIO MED: Inducible malignant ventricular tachyarrhythmia in a patient with genotyped hypertrophic cardiomyopathy in absence of left ventricular hypertrophy or enlargement.
|
19487599 |
2009 |
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
|
0.700 |
CausalMutation
|
CLINVAR |
Late gadolinium enhancement cardiovascular magnetic resonance in genotyped hypertrophic cardiomyopathy with normal phenotype.
|
19087273 |
2008 |
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
|
0.700 |
CausalMutation
|
CLINVAR |
Shared genetic causes of cardiac hypertrophy in children and adults.
|
18403758 |
2008 |
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
|
0.700 |
CausalMutation
|
CLINVAR |
Changes in the chemical and dynamic properties of cardiac troponin T cause discrete cardiomyopathies in transgenic mice.
|
16326803 |
2005 |
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
|
0.700 |
CausalMutation
|
CLINVAR |
Alterations in thin filament regulation induced by a human cardiac troponin T mutant that causes dilated cardiomyopathy are distinct from those induced by troponin T mutants that cause hypertrophic cardiomyopathy.
|
12186860 |
2002 |
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
|
0.700 |
CausalMutation
|
CLINVAR |
Ca(2+) activation of myofilaments from transgenic mouse hearts expressing R92Q mutant cardiac troponin T.
|
11158969 |
2001 |
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
|
0.700 |
CausalMutation
|
CLINVAR |
Disease-causing mutations in cardiac troponin T: identification of a critical tropomyosin-binding region.
|
11606294 |
2001 |
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
|
0.700 |
CausalMutation
|
CLINVAR |
Ca2+ sensitization and potentiation of the maximum level of myofibrillar ATPase activity caused by mutations of troponin T found in familial hypertrophic cardiomyopathy.
|
10085122 |
1999 |
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
|
0.700 |
CausalMutation
|
CLINVAR |
Cardiac troponin T mutations result in allele-specific phenotypes in a mouse model for hypertrophic cardiomyopathy.
|
10449439 |
1999 |
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
|
0.700 |
CausalMutation
|
CLINVAR |
Dominant-negative effect of a mutant cardiac troponin T on cardiac structure and function in transgenic mice.
|
9788962 |
1998 |
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
|
0.700 |
CausalMutation
|
CLINVAR |
Sudden death due to troponin T mutations.
|
9060892 |
1997 |
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
|
0.700 |
CausalMutation
|
CLINVAR |
Clinical manifestations of hypertrophic cardiomyopathy with mutations in the cardiac beta-myosin heavy chain gene or cardiac troponin T gene.
|
8951566 |
1996 |
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
|
0.700 |
CausalMutation
|
CLINVAR |
Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy.
|
7898523 |
1995 |
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
|
0.700 |
CausalMutation
|
CLINVAR |
Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere.
|
8205619 |
1994 |