Bujakowska et al., 2015 - Mutations in IFT172 Cause Isolated Retinal Degeneration and Bardet-Biedl Syndrome. Human molecular genetics   24(1):230-42 Full text @ Hum. Mol. Genet.

Fig. 5 ZFIN is incorporating published figure images and captions as part of an ongoing project. Figures from some publications have not yet been curated, or are not available for display because of copyright restrictions.

Full text @ Hum. Mol. Genet.