Clinical characteristics of 304 kindreds evaluated for familial dilated cardiomyopathy.
about
Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathyRare variant mutations identified in pediatric patients with dilated cardiomyopathyCoding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathyClinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathyCoding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathyFamilial dilated cardiomyopathy diagnosis is commonly overlooked at the time of transplant listing.Identification of novel mutations in RBM20 in patients with dilated cardiomyopathy.Rare variant mutations in pregnancy-associated or peripartum cardiomyopathy.Late onset sporadic dilated cardiomyopathy caused by a cardiac troponin T mutation.SCN5A rare variants in familial dilated cardiomyopathy decrease peak sodium current depending on the common polymorphism H558R and common splice variant Q1077del.Clinical and genetic issues in dilated cardiomyopathy: a review for genetics professionalsMutations of presenilin genes in dilated cardiomyopathy and heart failure.Functional characterization of TNNC1 rare variants identified in dilated cardiomyopathy.Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and diseaseLamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.Genetic testing for dilated cardiomyopathy in clinical practice.Cardiac magnetic resonance imaging of myocardial contrast uptake and blood flow in patients affected with idiopathic or familial dilated cardiomyopathyTemporal relationship of conduction system disease and ventricular dysfunction in LMNA cardiomyopathy.Return of genetic results in the familial dilated cardiomyopathy research projectDilated Cardiomyopathy Mutation (R134W) in Mouse Cardiac Troponin T Induces Greater Contractile Deficits against α-Myosin Heavy Chain than against β-Myosin Heavy Chain.Progress with genetic cardiomyopathies: screening, counseling, and testing in dilated, hypertrophic, and arrhythmogenic right ventricular dysplasia/cardiomyopathy.Family history of dilated cardiomyopathy among patients with heart failure from the HF-ACTION genetic ancillary study.Genetic evaluation of dilated cardiomyopathy.Toward Genetics-Driven Early Intervention in Dilated Cardiomyopathy: Design and Implementation of the DCM Precision Medicine Study.
P2860
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P2860
Clinical characteristics of 304 kindreds evaluated for familial dilated cardiomyopathy.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Clinical characteristics of 304 kindreds evaluated for familial dilated cardiomyopathy.
@ast
Clinical characteristics of 304 kindreds evaluated for familial dilated cardiomyopathy.
@en
type
label
Clinical characteristics of 304 kindreds evaluated for familial dilated cardiomyopathy.
@ast
Clinical characteristics of 304 kindreds evaluated for familial dilated cardiomyopathy.
@en
prefLabel
Clinical characteristics of 304 kindreds evaluated for familial dilated cardiomyopathy.
@ast
Clinical characteristics of 304 kindreds evaluated for familial dilated cardiomyopathy.
@en
P2093
P1476
Clinical characteristics of 304 kindreds evaluated for familial dilated cardiomyopathy.
@en
P2093
Deirdre Nauman
Donna Burgess
Emily Burkett
George Pantely
Jessica D Kushner
Ray E Hershberger
Sharie B Parks
Susan Ludwigsen
P304
P356
10.1016/J.CARDFAIL.2006.03.009
P577
2006-08-01T00:00:00Z