FIGURE SUMMARY
- Title
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Bi-allelic mutations in MYL1 cause a severe congenital myopathy
- Authors
- Ravenscroft, G., Zaharieva, I., Bortolotti, C.A., Lambrughi, M., Pignataro, M., Borsari, M., Sewry, C.A., Phadke, R., Haliloglu, G., Ong, R., Goullée, H., Whyte, T., UK10K Consortium, Manzur, A., Talim, B., Kaya, U., Osborn, D.P., Forrest, A., Laing, N.G., Muntoni, F.
- Source
- Full text @ Hum. Mol. Genet.
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:
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Acknowledgments