官方服务：
资源简介：
Familial Early-Onset Deep Venous Thrombosis Associated with a Novel HRG Mutation.
应用场景：
创建时间：
2017-09-25
相关数据集
A Novel Arginine to Tryptophan (R144W) Mutation in Troponin T (cTnT) Gene in an Indian Multigenerational Family with Dilated Cardiomyopathy (FDCM)
Cardiomyopathy is a major cause of heart failure and sudden cardiac death; several mutations in sarcomeric protein genes have been associated with this disease. Our aim in the present study is to inve
Figshare2016-01-15 更新40
Chi-Square and Mutual Information Profiling of SARS-CoV-2 Spike Mutation Clusters in a Comprehensive Global Dataset
This dataset presents the results of a large-scale statistical analysis of mutation co-occurrence patterns in the SARS-CoV-2 spike protein derived from 158,342 globally distributed viral genomes .
Zenodo2025-07-16 更新30
Correlation between PIK3CA, KRAS/PIK3CA/AKT mutation and hormone receptor status of 48 relapsed patients.
* Fisher’s exact testCorrelation between PIK3CA, KRAS/PIK3CA/AKT mutation and hormone receptor status of 48 relapsed patients.
Figshare2015-12-03 更新00
Histomorphological characteristics of lung adenocarcinoma based on driver mutation status.
Abbreviations: TN: triple negative.
NIAID Data Ecosystem30
Genetic variants associated with collagen VI deficient congenital muscular dystrophy in Labrador Retrievers
This project represents work aimed at identifying mutations associated with collagen VI congenital muscular dystrophy in young Labrador Retriever dogs.
NIAID Data Ecosystem00
