A locus for autosomal dominant mitral valve prolapse on chromosome 11p15.4.
about
Mitral valve disease--morphology and mechanisms.Epidemiology and pathophysiology of mitral valve prolapse: new insights into disease progression, genetics, and molecular basisMutations in DCHS1 cause mitral valve prolapseExpression of the familial cardiac valvular dystrophy gene, filamin-A, during heart morphogenesis.Mild expression of mitral valve prolapse in the Framingham offspring: expanding the phenotypic spectrum.Basic mechanisms of mitral regurgitation.Familial clustering of mitral valve prolapse in the community.Dynamic changes of the mitral valve annulus: new look at mitral valve diseases.Severity of Mitral Valve Degeneration Is Associated with Chromosome 15 Loci in Whippet Dogs.Targeted Mybpc3 Knock-Out Mice with Cardiac Hypertrophy Exhibit Structural Mitral Valve AbnormalitiesAutonomic dysregulation as a novel underlying cause of mitral valve prolapse: a hypothesisGenetic association analyses highlight biological pathways underlying mitral valve prolapse.Differential MicroRNA Expression Profile in Myxomatous Mitral Valve Prolapse and Fibroelastic Deficiency ValvesAbundance and location of proteoglycans and hyaluronan within normal and myxomatous mitral valvesMarfan syndrome and mitral valve prolapse.Heart valve structure and function in development and diseaseDegenerative mitral valve regurgitation: understanding basic concepts and new developments.Filamin-a-related myxomatous mitral valve dystrophy: genetic, echocardiographic and functional aspects.Mitral valve disease in Marfan syndrome and related disorders.Mendelian forms of structural cardiovascular disease.Myxomatous mitral valve disease bench to bedside: LDL-density-pressure regulates Lrp5.Mitral valve prolapse: a deeper look.Mitral Valve Prolapse: Multimodality Imaging and Genetic Insights.New insights into mitral valve dystrophy: a Filamin-A genotype-phenotype and outcome study.Genetics of syndromic and non-syndromic mitral valve prolapse.Investigation of the Matrix Metalloproteinase-2 Gene in Patients with Non-Syndromic Mitral Valve Prolapse.Imaging of Mitral Valve Prolapse: What Can We Learn from Imaging about the Mechanism of the Disease?Genomic analysis in patients with myxomatous mitral valve prolapse: current state of knowledge.Familial cardiac valvulopathy due to filamin A mutation.Screening of TGFBR1, TGFBR2, and FLNA in familial mitral valve prolapse.Fibrillin-1 gene intron 56 polymorphism in Turkish children with mitral valve prolapse.
P2860
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P2860
A locus for autosomal dominant mitral valve prolapse on chromosome 11p15.4.
description
2003 nî lūn-bûn
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2003 թուականի Ապրիլին հրատարակուած գիտական յօդուած
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2003 թվականի ապրիլին հրատարակված գիտական հոդված
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2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
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2003年论文
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name
A locus for autosomal dominant mitral valve prolapse on chromosome 11p15.4.
@ast
A locus for autosomal dominant mitral valve prolapse on chromosome 11p15.4.
@en
type
label
A locus for autosomal dominant mitral valve prolapse on chromosome 11p15.4.
@ast
A locus for autosomal dominant mitral valve prolapse on chromosome 11p15.4.
@en
prefLabel
A locus for autosomal dominant mitral valve prolapse on chromosome 11p15.4.
@ast
A locus for autosomal dominant mitral valve prolapse on chromosome 11p15.4.
@en
P2093
P2860
P356
P1476
A locus for autosomal dominant mitral valve prolapse on chromosome 11p15.4.
@en
P2093
Francesca Nesta
James S Acierno
Jane E Marshall
Lisa A Freed
Maire Leyne
Robert A Levine
Susan A Slaugenhaupt
P2860
P304
P356
10.1086/375452
P407
P577
2003-04-21T00:00:00Z