Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3

Alu repetitive elements are known to be major contributors to genome instability by generating Alu-mediated copy-number variants (CNVs). Most of the reported Alu-mediated CNVs are simple deletions and duplications, and the mechanism underlying Alu–Alu-mediated rearrangement has been attributed to no...

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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Hum Mol Genet
Egile Nagusiak: Gu, Shen, Yuan, Bo, Campbell, Ian M., Beck, Christine R., Carvalho, Claudia M.B., Nagamani, Sandesh C.S., Erez, Ayelet, Patel, Ankita, Bacino, Carlos A., Shaw, Chad A., Stankiewicz, Paweł, Cheung, Sau Wai, Bi, Weimin, Lupski, James R.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Oxford University Press 2015
Gaiak:
Articles
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4476451/
https://ncbi.nlm.nih.gov/pubmed/25908615
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddv146
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