Cite
HARVARD Citation
Scheidecker, S. et al. (2014). Exome sequencing of Bardet–Biedl syndrome patient identifies a null mutation in the BBSome subunit BBIP1 (BBS18). Journal of medical genetics. 51 (2), pp. 132-136. [Online].
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Scheidecker, S. et al. (2014). Exome sequencing of Bardet–Biedl syndrome patient identifies a null mutation in the BBSome subunit BBIP1 (BBS18). Journal of medical genetics. 51 (2), pp. 132-136. [Online].