- Loss-of-function mutation in Pcsk1 increases serum APOA1 level and LCAT activity in mice
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Khan AA, Kim N, Korstanje R, Choi S
- KMID: 2527819
- Lab Anim Res.
- 2022 Mar;38(1):18-26.
- doi: 10.1186/s42826-021-00111-2
Background: The convertase subtilisin/kexin family 1 gene (PCSK1) has been associated in various human genetics studies with a wide spectrum of metabolic phenotypes, including early-onset obesity, hyperphagia, diabetes insipidus, and... -
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