Targeted Exome Sequencing of Genes Involved in Rare CNVs in Early-Onset Severe Obesity

Context: Rare copy number variants (CNVs) have been associated with the development of severe obesity. However, the potential disease-causing contribution of individual genes within the region of CNVs is often not known. Objective: Screening of rare variants in genes involved in CNVs in Finnish pati...

Descripción completa

Detalles Bibliográficos
Autores principales: Loid, Petra, Pekkinen, Minna, Mustila, Taina, Tossavainen, Päivi, Viljakainen, Heli, Lindstrand, Anna, Mäkitie, Outi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8940233/
https://www.ncbi.nlm.nih.gov/pubmed/35330733
http://dx.doi.org/10.3389/fgene.2022.839349

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8940233/
https://www.ncbi.nlm.nih.gov/pubmed/35330733
http://dx.doi.org/10.3389/fgene.2022.839349

Ejemplares similares