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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Dettagli Bibliografici
Pubblicato in:NPJ Genom Med
Autori principali: Romdhane, Lilia, Mezzi, Nessrine, Dallali, Hamza, Messaoud, Olfa, Shan, Jingxuan, Fakhro, Khalid A., Kefi, Rym, Chouchane, Lotfi, Abdelhak, Sonia
Natura: Artigo
Lingua:Inglês
Pubblicazione: Nature Publishing Group UK 2021
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7794582/
https://ncbi.nlm.nih.gov/pubmed/33420067
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41525-020-00166-5
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