लोड हो रहा है...
Double jeopardy: long QT3 and Brugada syndromes
Mutations in the SCN5A gene are linked to both the long QT syndrome 3 and Brugada syndrome with few reports describing an overlapping phenotype. We present a unique case and discuss clinical considerations of a patient concurrently exhibiting such conditions with genetic analysis confirming an SCN5A...
में बचाया:
| में प्रकाशित: | Clin Case Rep |
|---|---|
| मुख्य लेखकों: | , , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
John Wiley and Sons Inc.
2017
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5538234/ https://ncbi.nlm.nih.gov/pubmed/28781849 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.1064 |
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