HRA002140
Title:
DEE56 in a Chinese family
Release date:
2022-03-21
Description:
We use trio-based whole-exome sequencing to search the etiology of a Chinese family with early-onset seizures, intellectual disability, and developmental delay.
Data Accessibility:   
Open access
BioProject:
Study type:
Disease Study
Disease name:
autosomal dominant disease
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Individuals & samples
Files
Submitter:   Zhang Ying / zhangying01225@163.com
Organization:   the Affiliated Hospital of Qingdao University
Submission date:   2022-03-18