Citations for
1BDP1, 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