View Tag: ‘Young’

Volume 9

A Canadian Collaboration Identifies the First Causative Gene, FOXL1, for Otosclerosis

Lucas et al write about a long-standing collaboration between Memorial University (Newfoundland and Labrador) and Western University (Ontario) that has leveraged the power of interdisciplinary expertise and large families to identify novel hearing loss genes.

Volume 3

Genomic Hearing Research and Development in Newfoundland

This article will tell you all about Newfoundland and Labrador’s Centre for Genomics-Based Research and Development in Hearing Science and its mission to facilitate discovery, innovation, and knowledge translation, with a focus on the genomic determinants of auditory dysfunction.