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CNVs cause autosomal recessive genetic diseases with or without involvement of SNV/indels

CNVs cause autosomal recessive genetic diseases with or without involvement of SNV/indels

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Bibliografske podrobnosti
Main Authors: Bo Yuan, Lei Wang, Pengfei Liu, Chad A. Shaw, Hongzheng Dai, Lance Cooper, Wenmiao Zhu, Stephanie A. Anderson, Linyan Meng, Xia Wang, Yue Wang, Fan Xia, Rui Xiao, Alicia Braxton, Sandra Peacock, Eric Schmitt, Patricia A. Ward, Francesco Vetrini, Weimin He, Theodore Chiang, Donna M. Muzny, Richard A. Gibbs, Arthur L. Beaudet, Amy M. Breman, Janice Smith, Sau Wai Cheung, Carlos A. Bacino, Christine M. Eng, Yaping Yang, James R. Lupski, Weimin Bi
Format: Artigo
Jezik:angleščina
Izdano: 2020
Online dostop:https://doi.org/10.1038/s41436-020-0864-8
http://www.gimjournal.org/article/S1098360021007528/pdf
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Internet

https://doi.org/10.1038/s41436-020-0864-8
http://www.gimjournal.org/article/S1098360021007528/pdf

Podobne knjige/članki

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  • The dynamic landscape of BRCA1 reversion mutations from indel to SNV in a patient with ovarian cancer treated with PARP-inhibitors and immunotherapy
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