Reducing Premature Coronary Artery Disease in Malaysia by Early Identification of Familial Hypercholesterolemia Using the Familial Hypercholesterolemia Case Ascertainment Tool (FAMCAT): Protocol for a Mixed Methods Evaluation Study

BACKGROUND: Familial hypercholesterolemia (FH) is predominantly caused by mutations in the 4 FH candidate genes (FHCGs), namely, low-density lipoprotein receptor (LDLR), apolipoprotein B-100 (APOB-100), proprotein convertase subtilisin/kexin type 9 (PCSK9), and the LDL receptor adaptor protein 1 (LD...

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Detalles Bibliográficos
Autores principales: Ramli, Anis Safura, Qureshi, Nadeem, Abdul-Hamid, Hasidah, Kamal, Aisyah, Kanchau, Johanes Dedi, Shahuri, Nur Syahirah, Akyea, Ralph Kwame, Silva, Luisa, Condon, Laura, Abdul-Razak, Suraya, Al-Khateeb, Alyaa, Chua, Yung-An, Mohamed-Yassin, Mohamed-Syarif, Baharudin, Noorhida, Badlishah-Sham, Siti Fatimah, Abdul Aziz, Aznida Firzah, Mohd Kasim, Noor Alicezah, Sheikh Abdul Kadir, Siti Hamimah, Kai, Joe, Leonardi-Bee, Jo, Nawawi, Hapizah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JMIR Publications 2023
Materias:
Protocol
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10276320/
https://www.ncbi.nlm.nih.gov/pubmed/37137823
http://dx.doi.org/10.2196/47911

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10276320/
https://www.ncbi.nlm.nih.gov/pubmed/37137823
http://dx.doi.org/10.2196/47911

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