Additional file 4: of Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes
Year: 2018
Type: dataset
Abstract: Table S1. which lists the software prediction tools used to call and annotate variants, with relevant references. (XLS 30 kb)
Source: Figshare
Language: English
Subfield: Sensory Systems
Field: Neuroscience
Domain: Life Sciences
Open Access status: green
OpenAlex ID: W4394371032