Dissecting Molecular Genetic Mechanisms of 1q21.1 CNV in Neuropsychiatric Disorders

Pathogenic copy number variations (CNVs) contribute to the etiology of neurodevelopmental/neuropsychiatric disorders (NDs). Increased CNV burden has been found to be critically involved in NDs compared with controls in clinical studies. The 1q21.1 CNVs, rare and large chromosomal microduplications a...

Descripción completa

Detalles Bibliográficos
Autores principales: Yoon, Joy, Mao, Yingwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8197994/
https://www.ncbi.nlm.nih.gov/pubmed/34071723
http://dx.doi.org/10.3390/ijms22115811

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8197994/
https://www.ncbi.nlm.nih.gov/pubmed/34071723
http://dx.doi.org/10.3390/ijms22115811

Ejemplares similares