The Genetic Spectrum of Familial Hypertriglyceridemia in Oman

Familial hypertriglyceridemia (F-HTG) is an autosomal disorder that causes severe elevation of serum triglyceride levels. It is caused by genetic alterations in LPL, APOC2, APOA5, LMF1, and GPIHBP1 genes. The mutation spectrum of F-HTG in Arabic populations is limited. Here, we report the genetic sp...

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Detalles Bibliográficos
Autores principales: Al-Waili, Khalid, Al-Rasadi, Khalid, Al-Bulushi, Muna, Habais, Mohammed, Al-Mujaini, Abdullah, Al-Yaarubi, Saif, Rimbert, Antoine, Zadjali, Razan, Khaniabadi, Pegah Moradi, Al-Barwani, Hamida, Hasary, Sana, Al-Dahmani, Zayana M., Al-Badi, Hala, Al-Maawali, Almundher, Zadjali, Fahad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9163817/
https://www.ncbi.nlm.nih.gov/pubmed/35669187
http://dx.doi.org/10.3389/fgene.2022.886182

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9163817/
https://www.ncbi.nlm.nih.gov/pubmed/35669187
http://dx.doi.org/10.3389/fgene.2022.886182

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