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- A nonsense loss-of-function mutation in PCSK1 contributes to dominantly inherited human obesity Academic Article
- Common nonsynonymous variants in PCSK1 confer risk of obesity Academic Article
- Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals Academic Article
- Heterozygous Mutations Causing Partial Prohormone Convertase 1 Deficiency Contribute to Human Obesity Academic Article
- How Effective Are Antioxidant Supplements in Obesity and Diabetes? Academic Article
- Re: "The Association of Common Variants in PCSK1 With Obesity: A HuGE Review and Meta-Analysis" Academic Article