Loading...
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...
Saved in:
| Published in: | Circ Arrhythm Electrophysiol |
|---|---|
| Main Authors: | , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
2015
|
| Subjects: | |
| Online Access: | 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 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|