Citations

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. (2020) Mutations in FASTKD2 are associated with mitochondrial disease with multi-OXPHOS deficiency. Human Mutation. 41(5):961-972

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. (2020) Mutations in FASTKD2 are associated with mitochondrial disease with multi-OXPHOS deficiency. Human Mutation. 41(5):961-972