Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions
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https://www.omicsdi.org/dataset/ega/EGAS00001007339
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Long-read whole genome sequencing, long-read long-range PCR sequencing, targetted long fragment long-read sequencing data of the CLCNKA/CLCNKB locus in 27 Bartter syndrome patients.
Multiple different deletion alleles are identified and a new common transposition haplotype predisposing for CLCNKB deletions is described.EGA study EGAS00001007339
创建时间:
2023-06-16



