Cite

    Scheidecker, S., Etard, C., Pierce, N. W., Geoffroy, V., Schaefer, E., Muller, J., Chennen, K., Flori, E., Pelletier, V., Poch, O., Marion, V., Stoetzel, C., Strähle, U., Nachury, M. V., & Dollfus, H. (2014). exome sequencing of Bardet–Biedl syndrome patient identifies a null mutation in the BBSome subunit BBIP1 (BBS18). Journal of medical genetics, 51(2), 132–136. http://access.bl.uk/ark:/81055/vdc_100137792994.0x000035