The Genetic Spectrum of Familial Hypertriglyceridemia in Oman.
LPL
familial hypertriglyceridemia
gene mutation
gene variant
lipoprotein lipase
Journal
Frontiers in genetics
ISSN: 1664-8021
Titre abrégé: Front Genet
Pays: Switzerland
ID NLM: 101560621
Informations de publication
Date de publication:
2022
2022
Historique:
received:
28
02
2022
accepted:
11
04
2022
entrez:
7
6
2022
pubmed:
8
6
2022
medline:
8
6
2022
Statut:
epublish
Résumé
Familial hypertriglyceridemia (F-HTG) is an autosomal disorder that causes severe elevation of serum triglyceride levels. It is caused by genetic alterations in
Identifiants
pubmed: 35669187
doi: 10.3389/fgene.2022.886182
pii: 886182
pmc: PMC9163817
doi:
Types de publication
Journal Article
Langues
eng
Pagination
886182Informations de copyright
Copyright © 2022 Al-Waili, Al-Rasadi, Al-Bulushi, Habais, Al-Mujaini, Al-Yaarubi, Rimbert, Zadjali, Khaniabadi, Al-Barwani, Hasary, Al-Dahmani, Al-Badi, Al-Maawali and Zadjali.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The handling editor FS declared a past co-authorship with the authors KAL, KAR, HAB, FZ.
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