FIGURE
Fig. S2
- ID
- ZDB-FIG-170831-1
- Publication
- Van De Weghe et al., 2017 - Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish
- Other Figures
- All Figure Page
- Back to All Figure Page
Fig. S2
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. |
Expression Data
Expression Detail
Antibody Labeling
Phenotype Data
| Fish: | |
|---|---|
| Knockdown Reagents: | |
| Observed In: | |
| Stage: | Adult |
Phenotype Detail
Acknowledgments