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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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| Udgivet i: | Mol Genet Genomic Med |
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| Main Authors: | , , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
John Wiley and Sons Inc.
2017
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| 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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