hum0202 Release Note
| Research ID | Release Date | Type of Data | 
|---|---|---|
| hum0202.v1 | 2022/09/09 | NGS (Exome) | 
hum0202.v1
DNAs extracted from peripheral blood cells of 3 congenital hearing loss patients and their parents were used for the whole exome sequencing analysis. 46 variants data are provided (xlsx).
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