QuickView for KRP;jsessionid=731619B62771E497F7AFE57452A8CD9F;jsessionid=E7F6F2A5F6D936FAB30A475870C11D71;jsessionid=511A0ED4A00B2BF031E2AEA8BFA321CA;jsessionid=9A9BCFD05ADDD61A04516421D02E3A9F;jsessionid=EA286A518AE2C5EBD83602A695AE0B76;jsessionid=FB6B2593E17B3A43652A80ED833CA3E0 (gene)

1. Contribution of heterozygous PCSK1 variants to obesity and implications for precision medicine: a ca…
2. A novel mutation of PCSK1 responsible for PC1/3 deficiency in two siblings.
3. Prader-Willi Syndrome and PCSK1 mutation: a novel presentation of combined syndromic and monogenic o…
4. Functional characterization of all missense variants in LEPR, PCSK1, and POMC genes arising from sin…
5. Association of PCSK1 gene polymorphisms with abdominal fat content in broilers.

There were no clinical trials for KRP;jsessionid=731619B62771E497F7AFE57452A8CD9F;jsessionid=E7F6F2A5F6D936FAB30A475870C11D71;jsessionid=511A0ED4A00B2BF031E2AEA8BFA321CA;jsessionid=9A9BCFD05ADDD61A04516421D02E3A9F;jsessionid=EA286A518AE2C5EBD83602A695AE0B76;jsessionid=FB6B2593E17B3A43652A80ED833CA3E0