Replication Data for: Characterization of a novel variant in the HR1 domain of MFN2 in a patient with ataxia, optic atrophy and sensorineural hearing loss

Name: Replication Data for: Characterization of a novel variant in the HR1 domain of MFN2 in a patient with ataxia, optic atrophy and sensorineural hearing loss
Creator: University of Calgary
Published: 2021-01-01T00:00:00+08:00

Harvard Dataverse2022-07-22 更新2026-04-09 收录

遗传病机制

基因变异功能分析

数据链接：

https://dataverse.harvard.edu/citation?persistentId=doi:10.7910/DVN/0R3C7S 数据链接链接失效反馈

官方服务：

资源简介：

Underlying data used to generate data for https://doi.org/10.1101/2021.01.11.426268.

提供机构：

University of Calgary

创建时间：

2021-01-01

Replication Data for: Characterization of a novel variant in the HR1 domain of MFN2 in a patient with ataxia, optic atrophy and sensorineural hearing loss

资源简介：

相关数据集