View Tag: ‘genetics’
Volume 9
A Canadian Collaboration Identifies the First Causative Gene, FOXL1, for Otosclerosis
by Matthew Lucas, PhD
Nelly Abdelfatah, MD, Ph.D.
Susan Stanton, PhD
Terry-Lynn Young, PhD
Anne Griffin, M.Sc. Audiology, R.Aud (NL)
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.