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We Only Find What We Look For: Fetal Heart Rate and the Diagnosis of Long QT Syndrome
Long QT syndrome (LQTS), an inherited channelopathy, is a common cause of arrhythmic death in infants, children and young adults. Although many LQTS genes have been identified, most (~75%) of LQTS mutations are found in KCNQ1, KCNH2 or SCN5A. In most cases, treatment for LQTS is successful and modif...
Tallennettuna:
| Julkaisussa: | Circ Arrhythm Electrophysiol |
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| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2015
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4552049/ https://ncbi.nlm.nih.gov/pubmed/26286300 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCEP.115.003196 |
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