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Identification of the MYH6 c.804G>C Synonymous Variant Causing Exon Skipping in a Hypertrophic Cardiomyopathy Family

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Published in:Molecular Genetics & Genomic Medicine
Format: Online Article RSS Article
Published: 2026
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container_title Molecular Genetics & Genomic Medicine
description
discipline_display Genetics
discipline_facet Genetics
format Online Article
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genre Journal Article
id rss_article:101553
institution FRELIP
journal_source_facet Molecular Genetics & Genomic Medicine
last_indexed 2026-07-10T03:36:23.074Z
publishDate 2026
publishDateSort 2026
record_format rss_article
spellingShingle Identification of the MYH6 c.804G>C Synonymous Variant Causing Exon Skipping in a Hypertrophic Cardiomyopathy Family
Genetics
General
Genetics
sub_discipline_display General
sub_discipline_facet General
subject_display Genetics
General
Genetics
subject_facet Genetics
General
Genetics
title Identification of the MYH6 c.804G>C Synonymous Variant Causing Exon Skipping in a Hypertrophic Cardiomyopathy Family
title_alt Identificación de la variante sinónima MYH6 c.804G>C que causa omisión de exón en una familia con miocardiopatía hipertrófica
Identification du variant synonyme MYH6 c.804G>C provoquant un saut d'exon dans une famille atteinte de cardiomyopathie hypertrophique
Identificação da variante sinônima MYH6 c.804G>C causando skipping de éxon em uma família com cardiomiopatia hipertrófica
title_auth Identification of the MYH6 c.804G>C Synonymous Variant Causing Exon Skipping in a Hypertrophic Cardiomyopathy Family
title_es_txt Identificación de la variante sinónima MYH6 c.804G>C que causa omisión de exón en una familia con miocardiopatía hipertrófica
title_fr_txt Identification du variant synonyme MYH6 c.804G>C provoquant un saut d'exon dans une famille atteinte de cardiomyopathie hypertrophique
title_full Identification of the MYH6 c.804G>C Synonymous Variant Causing Exon Skipping in a Hypertrophic Cardiomyopathy Family
title_fullStr Identification of the MYH6 c.804G>C Synonymous Variant Causing Exon Skipping in a Hypertrophic Cardiomyopathy Family
title_full_unstemmed Identification of the MYH6 c.804G>C Synonymous Variant Causing Exon Skipping in a Hypertrophic Cardiomyopathy Family
title_pt_txt Identificação da variante sinônima MYH6 c.804G>C causando skipping de éxon em uma família com cardiomiopatia hipertrófica
title_short Identification of the MYH6 c.804G>C Synonymous Variant Causing Exon Skipping in a Hypertrophic Cardiomyopathy Family
title_sort identification of the myh6 c.804g>c synonymous variant causing exon skipping in a hypertrophic cardiomyopathy family
topic Genetics
General
Genetics
url https://onlinelibrary.wiley.com/doi/10.1002/mgg3.70268?af=R