Heterozygous Genetic Variants in Autosomal Recessive Genes of the Leptin-Melanocortin Signalling Pathway Are Associated With the Development of Childhood Obesity

Monogenic obesity is a severe, genetically determined disorder that affects up to 1/1000 newborns. Recent reports on potential new therapeutics and innovative clinical approaches have highlighted the need for early identification of individuals with rare genetic variants that can alter the functioni...

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Detalles Bibliográficos
Autores principales: Šket, Robert, Kotnik, Primož, Bizjan, Barbara Jenko, Kocen, Valentina, Mlinarič, Matej, Tesovnik, Tine, Debeljak, Maruša, Battelino, Tadej, Kovač, Jernej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9105721/
https://www.ncbi.nlm.nih.gov/pubmed/35574020
http://dx.doi.org/10.3389/fendo.2022.832911

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9105721/
https://www.ncbi.nlm.nih.gov/pubmed/35574020
http://dx.doi.org/10.3389/fendo.2022.832911

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