1 | BDP1, DFNB112 |
Linkage study and exome sequencing identify a BDP1 mutation associated with hereditary hearing loss | |
Girotto G, Abdulhadi K, Buniello A, Vozzi D, Licastro D, d'Eustacchio A, Vuckovic D, Alkowari MK, Steel KP, Badii R, Gasparini P. | |
PLoS One. Dec 2;8(12):e80323. doi: 10.1371/journal.pone.0080323. 2013 | |