A Link between Genetic Disorders and Cellular Impairment, Using Human Induced Pluripotent Stem Cells to Reveal the Functional Consequences of Copy Number Variations in the Central Nervous System—A Close Look at Chromosome 15

Recent cutting-edge human genetics technology has allowed us to identify copy number variations (CNVs) and has provided new insights for understanding causative mechanisms of human diseases. A growing number of studies show that CNVs could be associated with physiological mechanisms linked to evolut...

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Detalles Bibliográficos
Autores principales: Casamassa, Alessia, Ferrari, Daniela, Gelati, Maurizio, Carella, Massimo, Vescovi, Angelo Luigi, Rosati, Jessica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7084702/
https://www.ncbi.nlm.nih.gov/pubmed/32182809
http://dx.doi.org/10.3390/ijms21051860

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7084702/
https://www.ncbi.nlm.nih.gov/pubmed/32182809
http://dx.doi.org/10.3390/ijms21051860

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