FIGURE SUMMARY
Title

A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly, epilepsy and autistic features.

Authors
Marin-Valencia, I., Novarino, G., Johansen, A., Rosti, B., Issa, M.Y., Musaev, D., Bhat, G., Scott, E., Silhavy, J.L., Stanley, V., Rosti, R.O., Gleeson, J.W., Imam, F.B., Zaki, M.S., Gleeson, J.G.
Source
Full text @ J. Med. Genet.
Fig. 2

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.

Fig. S5

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 / LABELING:
Gene:
Fish:
Anatomical Term:
Stage: Prim-5
PHENOTYPE:
Fish:
Knockdown Reagent:
Observed In:
Stage: Long-pec
Acknowledgments
Full text @ J. Med. Genet.
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