FIGURE

Fig. 4

ID

ZDB-FIG-170510-29

Publication

Osborn et al., 2017 - Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy

Other Figures

Fig. 3
Fig. 4
Fig. S1
Fig. S2
Fig. S3
Fig. S4

All Figure Page

Back to All Figure Page

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.

Expression Data

Expression Detail

Antibody Labeling

Phenotype Data

Fish:	AB + MO2-inpp5ka
Knockdown Reagent:	MO2-inpp5ka
Observed In:	myoseptum neuromuscular junction development, skeletal muscle fiber sarcomere organization skeletal muscle tissue development somite A band somite I band somite junctional membrane complex somite muscle cell
Stage:	Day 4

Phenotype Detail

Acknowledgments

Full text @ Am. J. Hum. Genet.