Variability in Inner Ear Morphology Among a Family With Pendred Syndrome Due to a SLC26A4 Gene Variant
YH Chen, WC Lin, CF Hwang, MH Tsai… - Annals of Otology … - journals.sagepub.com
Objectives: Pendred syndrome, an autosomal recessive disorder, is often associated with
pathogenic variants of the SLC26A4 gene that encodes the pendrin protein. Given its …
pathogenic variants of the SLC26A4 gene that encodes the pendrin protein. Given its …
Variability in Inner Ear Morphology Among a Family With Pendred Syndrome Due to a SLC26A4 Gene Variant
YH Chen, WC Lin, CF Hwang, MH Tsai… - The Annals of otology … - pubmed.ncbi.nlm.nih.gov
Objectives Pendred syndrome, an autosomal recessive disorder, is often associated with
pathogenic variants of the SLC26A4 gene that encodes the pendrin protein. Given its …
pathogenic variants of the SLC26A4 gene that encodes the pendrin protein. Given its …