Resequencing Genomic DNA of Patients With Severe Hypertriglyceridemia (MIM 144650) | Zendy

Jian Wang | Zendy; Henian Cao | Zendy; Matthew R. Ban | Zendy; Brooke A. Kennedy | Zendy; Siqi Zhu | Zendy; Sonia S. Anand | Zendy; Salim Yusuf | Zendy; Rebecca L. Pollex | Zendy; Robert A. Hegele | Zendy

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Resequencing Genomic DNA of Patients With Severe Hypertriglyceridemia (MIM 144650)

Author(s) -

Jian Wang,

Henian Cao,

Matthew R. Ban,

Brooke A. Kennedy,

Siqi Zhu,

Sonia S. Anand,

Salim Yusuf,

Rebecca L. Pollex,

Robert A. Hegele

Publication year - 2007

Publication title -

arteriosclerosis thrombosis and vascular biology

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 3.007

H-Index - 270

eISSN - 1524-4636

pISSN - 1079-5642

DOI - 10.1161/atvbaha.107.150680

Subject(s) - missense mutation , hypertriglyceridemia , genetics , odds ratio , biology , medicine , endocrinology , gene , mutation , triglyceride , cholesterol

The genetic determinants of severe hypertriglyceridemia (HTG; MIM 144650) in adults are poorly defined. We therefore resequenced 3 candidate genes, namely LPL, APOC2, and APOA5, to search for accumulation of missense mutations in patients with severe HTG compared with normolipidemic subjects.

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