Familial dilated cardiomyopathy locus maps to chromosome 2q31.
about
Cardiomyopathy classification: ongoing debate in the genomics eraConstitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathyHomozygosity 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 cardiomyopathyTibial muscular dystrophy is a titinopathy caused by mutations in TTN, the gene encoding the giant skeletal-muscle protein titinGenetic epidemiology of titin-truncating variants in the etiology of dilated cardiomyopathy.Wolff-Parkinson-White Syndrome with Ventricular Hypertrophy in a Brazilian Family.Genetic abnormalities responsible for dilated cardiomyopathy.Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22.Molecular dissection of N2B cardiac titin's extensibilityTruncations of titin causing dilated cardiomyopathy.Muscle giants: molecular scaffolds in sarcomerogenesis.Molecular mechanisms of inherited cardiomyopathies.Molecular diagnosis of myocardial disease.Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and diseaseTitin: physiological function and role in cardiomyopathy and failure.Genetics of dilated cardiomyopathy.Genetic profiling for risk reduction in human cardiovascular disease.A 56-year-old man with co-prevalence of Leriche syndrome and dilated cardiomyopathy: case report and review.Almanac 2014: cardiomyopathies.LITTLE FISH, BIG DATA: ZEBRAFISH AS A MODEL FOR CARDIOVASCULAR AND METABOLIC DISEASE.Truncating titin mutations are associated with a mild and treatable form of dilated cardiomyopathy.Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy.Stressing the giant: a new approach to understanding dilated cardiomyopathy.Evidence for autosomal recessive inheritance of infantile dilated cardiomyopathy: studies from the Eastern Province of Saudi Arabia.Genome-wide linkage scan for exercise stroke volume and cardiac output in the HERITAGE Family Study.Conditional expression of mutant M-line titins results in cardiomyopathy with altered sarcomere structure.Next generation sequencing applications for cardiovascular disease.Using Gene Expression to Annotate Cardiovascular GWAS Loci.Titins
P2860
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P2860
Familial dilated cardiomyopathy locus maps to chromosome 2q31.
description
1999 nî lūn-bûn
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1999 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի մարտին հրատարակված գիտական հոդված
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1999年の論文
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1999年学术文章
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1999年学术文章
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1999年学术文章
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1999年学术文章
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1999年学术文章
@zh-sg
1999年學術文章
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name
Familial dilated cardiomyopathy locus maps to chromosome 2q31.
@ast
Familial dilated cardiomyopathy locus maps to chromosome 2q31.
@en
type
label
Familial dilated cardiomyopathy locus maps to chromosome 2q31.
@ast
Familial dilated cardiomyopathy locus maps to chromosome 2q31.
@en
prefLabel
Familial dilated cardiomyopathy locus maps to chromosome 2q31.
@ast
Familial dilated cardiomyopathy locus maps to chromosome 2q31.
@en
P2093
P356
P1433
P1476
Familial dilated cardiomyopathy locus maps to chromosome 2q31.
@en
P2093
Osborne JA
Seidman CE
Seidman JG
P304
P356
10.1161/01.CIR.99.8.1022
P407
P577
1999-03-01T00:00:00Z