FIGURE

Fig. S18

ID

ZDB-FIG-241106-12

Publication

Brugger et al., 2024 - Bi-allelic variants in SNF8 cause a disease spectrum ranging from severe developmental and epileptic encephalopathy to syndromic optic atrophy

Other Figures

Fig. S18
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Fig. S18

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Expression Data

Expression Detail

Antibody Labeling

Phenotype Data

Fish:	NHGRI-1 + MO1-snf8 + MO4-tp53
Knockdown Reagents:	MO1-snf8 MO4-tp53
Observed In:	eye head integument post-vent region
Stage:	Prim-5

Phenotype Detail

Acknowledgments

This image is the copyrighted work of the attributed author or publisher, and ZFIN has permission only to display this image to its users. Additional permissions should be obtained from the applicable author or publisher of the image. Full text @ Am. J. Hum. Genet.