Novel EYA1 variants causing Branchio-oto-renal syndrome

Article

Abstract: Introduction Branchio-oto-renal (BOR) syndrome is an autosomal dominant genetic disorder characteriz

Palabras claves:

Branchial arch anomalies, Branchiootorenal syndrome, EYA1, hearing loss, Whole exome sequencing

Autores:

Arianne Llamos Paneque, Arslan S., Bademci G., Behnam M., Carrera-Gonzalez A., Cengiz F.B., Demir Ulusal S., Duman D., Elcioglu N., Escarfuller S., Foster J., Greenland C.M., Guo S., Gurkan H., Klingbeil K.D., Maroofian R., Menendez I., Montufar-Armendariz S., Paredes R., Tekin M.

Fuentes:

scopus