FIGURE SUMMARY
Title

Homozygous splice mutation in CWF19L1 in a Turkish family with recessive ataxia syndrome

Authors
Burns, R., Majczenko, K., Xu, J., Peng, W., Yapici, Z., Dowling, J.J., Li, J.Z., Burmeister, M.
Source
Full text @ Neurology
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.

PHENOTYPE:
Fish:
Knockdown Reagents:
Observed In:
Stage Range: Protruding-mouth to Day 5
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.

PHENOTYPE:
Fish:
Knockdown Reagent:
Observed In:
Stage: Day 5
Acknowledgments
Full text @ Neurology
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