A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North Africa

Copy number variation (CNV) is considered as the most frequent type of structural variation in the human genome. Some CNVs can act on human phenotype diversity, encompassing rare Mendelian diseases and genomic disorders. The North African populations remain underrepresented in public genetic databas...

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Detalles Bibliográficos
Autores principales: Romdhane, Lilia, Mezzi, Nessrine, Dallali, Hamza, Messaoud, Olfa, Shan, Jingxuan, Fakhro, Khalid A., Kefi, Rym, Chouchane, Lotfi, Abdelhak, Sonia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7794582/
https://www.ncbi.nlm.nih.gov/pubmed/33420067
http://dx.doi.org/10.1038/s41525-020-00166-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7794582/
https://www.ncbi.nlm.nih.gov/pubmed/33420067
http://dx.doi.org/10.1038/s41525-020-00166-5

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