mirDNMR: a gene-centered database of background de novo mutation rates in human

De novo germline mutations (DNMs) are the rarest genetic variants proven to cause a considerable number of sporadic genetic diseases, such as autism spectrum disorders, epileptic encephalopathy, schizophrenia, congenital heart disease, type 1 diabetes, and hearing loss. However, it is difficult to a...

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Detalles Bibliográficos
Autores principales: Jiang, Yi, Li, Zhongshan, Liu, Zhenwei, Chen, Denghui, Wu, Wanying, Du, Yaoqiang, Ji, Liying, Jin, Zi-Bing, Li, Wei, Wu, Jinyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Database Issue
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5210538/
https://www.ncbi.nlm.nih.gov/pubmed/27799474
http://dx.doi.org/10.1093/nar/gkw1044

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5210538/
https://www.ncbi.nlm.nih.gov/pubmed/27799474
http://dx.doi.org/10.1093/nar/gkw1044

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