Grati et al., 2015 - A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation. Human molecular genetics   24(9):2482-91 Full text @ Hum. Mol. Genet.

Fig. 4 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.

Unillustrated author statements

Knockdown Reagent:
Observed In:
Stage: Protruding-mouth
Full text @ Hum. Mol. Genet.