Keeping It in the Family: Consanguinity Reveals P4HTM as a Novel Syndromic Obesity Gene
- PMID: 37603723
- PMCID: PMC10450820
- DOI: 10.2337/dbi23-0010
Keeping It in the Family: Consanguinity Reveals P4HTM as a Novel Syndromic Obesity Gene
Conflict of interest statement
Comment on
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Biallelic Mutations in P4HTM Cause Syndromic Obesity.Diabetes. 2023 Sep 1;72(9):1228-1234. doi: 10.2337/db22-1017. Diabetes. 2023. PMID: 37083980 Free PMC article.
References
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- Daniels SR, Arnett DK, Eckel RH, et al. . Overweight in children and adolescents: pathophysiology, consequences, prevention, and treatment. Circulation 2005;111:1999–2012 - PubMed
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