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Deleterious variants in DCHS1 are prevalent in sporadic cases of mitral valve prolapse

BACKGROUND: A recent study identified DCHS1 as a causal gene for mitral valve prolapse. The goal of this study is to investigate the presence and frequency of known and novel variants in this gene in 100 asymptomatic patients with moderate to severe organic mitral regurgitation. METHODS: DNA sequenc...

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Bibliografiske detaljer
Udgivet i:Mol Genet Genomic Med
Main Authors: Clemenceau, Alisson, Bérubé, Jean‐Christophe, Bélanger, Paméla, Gaudreault, Nathalie, Lamontagne, Maxime, Toubal, Oumhani, Clavel, Marie‐Annick, Capoulade, Romain, Mathieu, Patrick, Pibarot, Philippe, Bosse, Yohan
Format: Artigo
Sprog:Inglês
Udgivet: John Wiley and Sons Inc. 2017
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5823682/
https://ncbi.nlm.nih.gov/pubmed/29224215
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.347
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