Sanger sequencing-data
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资源简介：
This dataset includes Sanger sequencing chromatograms (.ab1 files) corresponding to the validation of candidate variants identified through exome sequencing in four Iranian non-syndromic hearing loss (NSHL) families. The files represent electropherograms for affected and unaffected family members used to confirm segregation of the identified variants.<br>All data were anonymized to protect patient confidentiality.<br>
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figshare创建时间：
2025-11-06
