Case-finding and genetic testing for familial hypercholesterolaemia in primary care
Objective Familial hypercholesterolaemia (FH) is a common inherited disorder that remains mostly undetected in the general population. Through FH case-finding and direct access to genetic testing in primary care, this intervention study described the genetic and lipid profile of patients found at in...
| Published in: | Heart |
|---|---|
| Main Author: | |
| Format: | Article |
| Language: | English |
| Published: |
BMJ Publishing Group
2021
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| Online Access: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85120546710&doi=10.1136%2fheartjnl-2021-319742&partnerID=40&md5=78a56f6500c7e1cd47ffa7abf7aea53a |