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MOESM5 of Association of CMV genomic mutations with symptomatic infection and hearing loss in congenital CMV infection

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posted on 2019-12-11, 10:42 authored by G. Dobbins, Amit Patki, Dongquan Chen, Hemant Tiwari, Curtis Hendrickson, William Britt, Karen Fowler, Jake Chen, Suresh Boppana, Shannon Ross
Additional file 5: Table S4. Non-parametric test comparing CMV nucleotide diversity by gene in samples between infants with normal hearing and those with SNHL.

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National Institutes of Health

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