Latest Physician Education Resources
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
Ouabain induces transcript changes and activation of RhoA/ROCK signaling in cultured epithelial cells (MDCK)
