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 i...

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Bibliographic Details
Main Authors: Abdul Hamid, H. (Author), Akyea, R.K (Author), Condon, L. (Author), Dutton, B. (Author), FAMCAT study (Author), Humphries, S.E (Author), Kai, J. (Author), Qureshi, N. (Author), Weng, S.F (Author)
Format: Article
Language:English
Published: NLM (Medline) 2021
Series:Heart (British Cardiac Society)
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