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Paper Details

Common and Rare Genetic Variants That Could Contribute to Severe Otitis Media in an Australian Aboriginal Population.
Clin Infect Dis
2
2021
ARSA, CDH23, EYA4, FAT4, FGFR1, GRXCR1, Genetic Variants, Illumina Omni2, LMNA, LRP2, MYO7A, NR3C1, NREP, OM, Otitis Media, abnormal, abnormal ear, acute OM, children, chronic suppurative OM, gene, gene-sets, genes, genetic risk loci, glucocorticoid receptor, hair cell stereociliary bundles, integrin, interacting genes, neuronal regeneration-related protein, otitis media, transforming growth factor, tympanic sclerosis
Author NameAffiliation
Timo LassmannTelethon Kids Institute, The University of Western Australia
Timo LassmannTelethon Kids Institute, The University of Western Australia
Heather J CordellPopulation Health Sciences Institute, Newcastle University
Jenefer M BlackwellTelethon Kids Institute, The University of Western Australia
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Datasets

Release 1.2