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Thompson K, Majd H, Dallabona C, et al. Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number. Am J Hum Genet. 2016;99(6):1405doi: 10.1016/j.ajhg.2016.11.001.
Thompson, K., Majd, H., Dallabona, C., Reinson, K., King, M. S., Alston, C. L., He, L., Lodi, T., Jones, S. A., Fattal-Valevski, A., Fraenkel, N. D., Saada, A., Haham, A., Isohanni, P., Vara, R., Barbosa, I. A., Simpson, M. A., Deshpande, C., Puusepp, S., Bonnen, P. E., Rodenburg, R. J., Suomalainen, A., Õunap, K., Elpeleg, O., Ferrero, I., McFarland, R., Kunji, E. R. S., & Taylor, R. W. (2016). Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number. American journal of human genetics, 99(6), 1405. https://doi.org/10.1016/j.ajhg.2016.11.001
Thompson, Kyle, et al. "Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number." American journal of human genetics vol. 99,6 (2016): 1405. doi: https://doi.org/10.1016/j.ajhg.2016.11.001
Thompson K, Majd H, Dallabona C, Reinson K, King MS, Alston CL, He L, Lodi T, Jones SA, Fattal-Valevski A, Fraenkel ND, Saada A, Haham A, Isohanni P, Vara R, Barbosa IA, Simpson MA, Deshpande C, Puusepp S, Bonnen PE, Rodenburg RJ, Suomalainen A, Õunap K, Elpeleg O, Ferrero I, McFarland R, Kunji ERS, Taylor RW. Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number. Am J Hum Genet. 2016 Dec 01;99(6):1405. doi: 10.1016/j.ajhg.2016.11.001. PMID: 27912046; PMCID: PMC5142113.
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