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Article

Filamin A mitral valve disease: prolapse, dystrophy, or dysplasia?

European heart journal - 14 Apr 2018

Thiene Gaetano, Basso Cristina

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Share to Filamins
Share to Genotype
Share to Mitral Valve
Share to Mitral Valve Prolapse

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Phenotype

Source

Identifiers

PMID: 29040517
DOI: 10.1093/eurheartj/ehx578

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

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Research trail→

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Filamin A mitral valve disease: prolapse, dystrophy, or dysplasia?PMID 29040517Read ↗

New insights into mitral valve dystrophy: a Filamin-A genotype-phenotype and outcome study.Semantic proximity Read ↗

Valve-sparing Aortic Root Replacement for a Patient With Filamin A Mutation.Semantic proximity Read ↗

Filamin-a-related myxomatous mitral valve dystrophy: genetic, echocardiographic and functional aspects.Semantic proximity Read ↗

Genetics of syndromic and non-syndromic mitral valve prolapse.Semantic proximity Read ↗

Expression of the familial cardiac valvular dystrophy gene, filamin‐A, during heart morphogenesisSemantic proximity Read ↗

Filamin A heart valve disease as a genetic cause of inherited bicuspid and tricuspid aortic valve diseaseSemantic proximity Read ↗

Isolated prolapse of the posterior mitral valve leaflet: phenotypic refinement, heritability and genetic etiologySemantic proximity Read ↗

Molecular genetics of mitral valve prolapse.Semantic proximity Read ↗

Developmental basis for filamin-A-associated myxomatous mitral valve diseaseSemantic proximity Read ↗

Familial cardiac valvulopathy due to filamin A mutation.Semantic proximity Read ↗

Filamin A: phenotypic diversity.Semantic proximity Read ↗

Mutations in the gene encoding filamin A as a cause for familial cardiac valvular dystrophy.Semantic proximity Read ↗

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