12879_2019_4681_MOESM4_ESM.xlsx (86.61 kB)
MOESM4 of Association of CMV genomic mutations with symptomatic infection and hearing loss in congenital CMV infection
dataset
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 RossAdditional file 4: Table S3. Table of CMV variants more common in symptomatic children. The accession number prefix is listed; and nomenclature used for reporting is taken from http://www.hgvs.org/mutnomen/.
