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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Detalles Bibliográficos
Autores principales: Clemenceau, Alisson, Bérubé, Jean‐Christophe, Bélanger, Paméla, Gaudreault, Nathalie, Lamontagne, Maxime, Toubal, Oumhani, Clavel, Marie‐Annick, Capoulade, Romain, Mathieu, Patrick, Pibarot, Philippe, Bosse, Yohan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Clinical Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5823682/
https://www.ncbi.nlm.nih.gov/pubmed/29224215
http://dx.doi.org/10.1002/mgg3.347

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5823682/
https://www.ncbi.nlm.nih.gov/pubmed/29224215
http://dx.doi.org/10.1002/mgg3.347

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