- Title
-
Mutations in FASTKD2 are associated with mitochondrial disease with multi-OXPHOS deficiency
- Authors
- Wei, X., Du, M., Li, D., Wen, S., Xie, J., Li, Y., Chen, A., Zhang, K., Xu, P., Jia, M., Wen, C., Zhou, H., Lyu, J., Yang, Y., Fang, H.
- Source
- Full text @ Hum. Mutat.
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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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:
|
|
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:
|