FIGURE SUMMARY
Title

Mutation of the mitochondrial carrier SLC25A42 causes a novel form of mitochondrial myopathy in humans

Authors
Shamseldin, H.E., Smith, L.L., Kentab, A., Alkhalidi, H., Summers, B., Alsedairy, H., Xiong, Y., Gupta, V.A., Alkuraya, F.S.
Source
Full text @ Hum. Genet.
Fig. 3

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. 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.

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.

Acknowledgments
Full text @ Hum. Genet.
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