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PITX2C loss-of-function mutations responsible for idiopathic atrial fibrillation
OBJECTIVE: This study aimed to identify novel PITX2c mutations responsible for idiopathic atrial fibrillation. METHODS: A cohort of 210 unrelated patients with idiopathic atrial fibrillation and 200 unrelated, ethnically matched healthy individuals used as controls were recruited. The whole coding e...
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| Hoofdauteurs: | , , , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
2014
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3870307/ https://ncbi.nlm.nih.gov/pubmed/24473555 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6061/clinics/2014(01)03 |
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