GPCards: An integrated database of genotype–phenotype correlations in human genetic diseases

Genotype–phenotype correlations are the basis of precision medicine of human genetic diseases. However, it remains a challenge for clinicians and researchers to conveniently access detailed individual-level clinical phenotypic features of patients with various genetic variants. To address this urgen...

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Detalles Bibliográficos
Autores principales: Li, Bin, Wang, Zheng, Chen, Qian, Li, Kuokuo, Wang, Xiaomeng, Wang, Yijing, Zeng, Qian, Han, Ying, Lu, Bin, Zhao, Yuwen, Zhang, Rui, Jiang, Li, Pan, Hongxu, Luo, Tengfei, Zhang, Yi, Fang, Zhenghuan, Xiao, Xuewen, Zhou, Xun, Wang, Rui, Zhou, Lu, Wang, Yige, Yuan, Zhenhua, Xia, Lu, Guo, Jifeng, Tang, Beisha, Xia, Kun, Zhao, Guihu, Li, Jinchen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2021
Materias:
Data Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8042245/
https://www.ncbi.nlm.nih.gov/pubmed/33868597
http://dx.doi.org/10.1016/j.csbj.2021.03.011

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8042245/
https://www.ncbi.nlm.nih.gov/pubmed/33868597
http://dx.doi.org/10.1016/j.csbj.2021.03.011

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