CORC

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CORC

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Japanese Encephalitis Virus NS1 Protein Antagonizes Interferon Beta Production 期刊论文
VIROLOGICA SINICA, 2018, 卷号: 33, 期号: 6, 页码: 515-523
作者:  Ye, Jing;  Cao, Shengbo;  Chen, Huanchun;  Song, Yunfeng;  Cui, Min
收藏  |  浏览/下载：58/0  |  提交时间：2019/06/24
Targeted Next-Generation Sequencing Reveals a Novel Frameshift Mutation in the MERTK Gene in a Chinese Family with Retinitis Pigmentosa 期刊论文
GENETIC TESTING AND MOLECULAR BIOMARKERS, 2018, 卷号: 22, 期号: 3, 页码: 165-169
作者:  Yang, Mu;  Li, Shujin;  Liu, Wenjing;  Yang, Yeming;  Zhang, Lin
收藏  |  浏览/下载：20/0  |  提交时间：2020/12/24
Novel HOXD13 frameshift mutation causes synpolydactyly and clinodactyly 期刊论文
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE, 2018, 卷号: 11, 期号: 10
作者:  Ni, Feng;  Han, Gang;  Guo, Ruiji;  An, Yu;  Wang, Bin
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/05
A novel frameshift SERPINB7 mutation in a Chinese case with Nagashima-type palmoplantar keratosis: case report and review of the literature 期刊论文
CLINICAL AND EXPERIMENTAL DERMATOLOGY, 2018, 卷号: 43, 期号: 8
作者:  Hua, S.;  Miao, X.;  Mao, W.;  Hua, L.;  Chen, J.
收藏  |  浏览/下载：2/0  |  提交时间：2019/12/05
A novel frameshift SERPINB7 mutation in a Chinese case with Nagashima-type palmoplantar keratosis: case report and review of the literature 期刊论文
Clinical and experimental dermatology, 2018, 卷号: 43, 页码: 953-955
作者:  Hua S[1];  Miao X[2];  Mao W[3];  Hua L[4];  Chen J[5]
收藏  |  浏览/下载：5/0  |  提交时间：2019/04/22
A novel splicing mutation in the PKD1 gene causes autosomal dominant polycystic kidney disease in a Chinese family: a case report 期刊论文
BMC MEDICAL GENETICS, 2018, 卷号: 19, 期号: 1
作者:  Xu, Peiwen;  Huang, Sexing;  Li, Jie;  Zou, Yang;  Gao, Ming
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/11
c. 1439delA frameshift deletion mutation in familial adenomatous polyposis 期刊论文
ONCOTARGETS AND THERAPY, 2018, 卷号: 11, 页码: 8987-8993
作者:  Ma, De-Jian;  Wang, Bi-Shi;  Yue, Jin-Bo;  Li, Zeng-Jun;  Sun, Yan-Lai
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/11
Case report of a novel PCDH19 frameshift mutation in a girl with epilepsy and mental retardation limited to females 期刊论文
MEDICINE, 2018, 卷号: 97, 期号: 51
作者:  Zhang, Xinying;  Chen, Na;  Ma, Aihua;  Wang, Xueyu;  Sun, Wenxiu
收藏  |  浏览/下载：11/0  |  提交时间：2019/12/11
A novel splicing mutation in the PKD1 gene causes autosomal dominant polycystic kidney disease in a Chinese family: a case report 期刊论文
BMC Medical Genetics, 2018, 卷号: Vol.19 No.1, 页码: 1-6
作者:  Peiwen Xu;  Sexing Huang;  Jie Li;  Yang Zou;  Ming Gao
收藏  |  浏览/下载：17/0  |  提交时间：2019/12/26
A novel CRX frameshift mutation causing cone-rod dystrophy in a Chinese family: A case report 期刊论文
2018, 卷号: 97, 期号: 32, 页码: e11499
作者:  Wang, Lihua;  Qi, Anhui;  Pan, Hong;  Liu, Beihong;  Feng, Jingjing
收藏  |  浏览/下载：4/0  |  提交时间：2020/01/03

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