Latest Physician Education Resources

Expansion of phenotypic spectrum of MYO15A pathogenic variants to include postlingual onset of progressive partial deafness

An Annual Cycle of Gene Regulation in the Red-Legged Salamander Mental Gland: From Hypertrophy to Expression Of Rapidly Evolving Pheromones

Transcriptome Profiling of Neovascularized Corneas Reveals miR-204 as a Multi-target Biotherapy Deliverable by rAAVs

Precision Medicine in Hearing Loss

The Genetics of Usher Syndrome in the Israeli and Palestinian Populations

A Missense Mutation in pou4f3 Causes Mid-Frequency Hearing Loss in a Chinese ADNSHL Family

A Novel Pathogenic Variant in the MARVELD2 Gene Causes Autosomal Recessive Non-syndromic Hearing Loss in an Iranian Family

Novel Poxvirus in Proliferative Lesions of Wild Rodents in East Central Texas, USA

Whole‐Exome Sequencing for Variant Discovery in Blepharospasm

Missense variant of endoplasmic reticulum region of WFS1 gene causes autosomal dominant hearing loss without syndromic phenotype

Nkx2.3 Transcription factor is a key regulator of mucous cell identity in salivary glands

Dominant frontonasal dysplasia with ectodermal defects results from increased activity of ALX4