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Homozygosity mapping and exome sequencing reveal GATAD1 mutation in autosomal recessive dilated cardiomyopathyA new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16Many roads lead to a broken heart: the genetics of dilated cardiomyopathy.Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathyThe cell biology of disease: cellular mechanisms of cardiomyopathy.Mutational analysis of the beta- and delta-sarcoglycan genes in a large number of patients with familial and sporadic dilated cardiomyopathyPolycystin-2 mutations lead to impaired calcium cycling in the heart and predispose to dilated cardiomyopathyFamilial dilated cardiomyopathy diagnosis is commonly overlooked at the time of transplant listing.Genetic aspects of heart failure.Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22.A proton leak current through the cardiac sodium channel is linked to mixed arrhythmia and the dilated cardiomyopathy phenotype.Animal models of cardiac disease and stem cell therapy.Genes and their polymorphisms in mono- and multifactorial cardiomyopathies: towards pharmacogenomics in heart failure.Mutations in the Z-band protein myopalladin gene and idiopathic dilated cardiomyopathy.Molecular mechanisms of inherited cardiomyopathies.Cardiomyopathy, familial dilated.Cardiac autoimmunity in HIV related heart muscle disease.Haemochromatosis gene mutations in idiopathic dilated cardiomyopathy.Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations.Abnormal cardiopulmonary exercise variables in asymptomatic relatives of patients with dilated cardiomyopathy who have left ventricular enlargementProgression of familial and non-familial dilated cardiomyopathy: long term follow up.Genetics of inherited cardiomyopathies.Impact of Mendelian inheritance in cardiovascular disease.Genetic variation in the alternative splicing regulator RBM20 is associated with dilated cardiomyopathy.Genetics of dilated cardiomyopathy.Idiopathic dilated cardiomyopathy: familial prevalence and HLA distributionEvolving molecular diagnostics for familial cardiomyopathies: at the heart of it allMapping a cardiomyopathy locus to chromosome 3p22-p25.Mutations in ribonucleic acid binding protein gene cause familial dilated cardiomyopathy.Beyond membrane channelopathies: alternative mechanisms underlying complex human disease.Mendelian forms of structural cardiovascular disease.Familial dilated cardiomyopathy: clinical features in French families.Formation of a TBX20-CASZ1 protein complex is protective against dilated cardiomyopathy and critical for cardiac homeostasis.Dilated cardiomyopathy: a genetic approach.Fractal correlation properties of R-R interval dynamics in asymptomatic relatives of patients with dilated cardiomyopathy.Genetic and phenotypic analysis of dilated cardiomyopathy with conduction system disease: demand for strategies in the management of presymptomatic lamin A/C mutant carriers.Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene
P2860
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P2860
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
1995年论文
@zh
1995年论文
@zh-cn
name
Familial dilated cardiomyopathy in the United Kingdom.
@ast
Familial dilated cardiomyopathy in the United Kingdom.
@en
type
label
Familial dilated cardiomyopathy in the United Kingdom.
@ast
Familial dilated cardiomyopathy in the United Kingdom.
@en
prefLabel
Familial dilated cardiomyopathy in the United Kingdom.
@ast
Familial dilated cardiomyopathy in the United Kingdom.
@en
P2093
P2860
P356
P1476
Familial dilated cardiomyopathy in the United Kingdom.
@en
P2093
Caforio AL
Keeling PJ
McKenna WJ
P2860
P304
P356
10.1136/HRT.73.5.417
P577
1995-05-01T00:00:00Z