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Open Access UCL Research: Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions https://t.co/LWyRP2v4X1
Open Access UCL Research: Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions https://t.co/LWyRP2v4X1
RT @elfridedebaere: https://t.co/2QPZagQ6Su @GenomeMedicine
https://t.co/2QPZagQ6Su @GenomeMedicine
How @berlinnovation and @MDC_Berlin mapped out a rare kidney disease known as Bartter syndrome type 3. Read their new findings here: https://t.co/NXxgR8XDCj ~~ #GenomicMedicine #Sequencing #RareDisease