Cite
HARVARD Citation
Belal, H. et al. (2018). De novo variants in RHOBTB2, an atypical Rho GTPase gene, cause epileptic encephalopathy. Human mutation. 39 (8), pp. 1070-1075. [Online].
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Belal, H. et al. (2018). De novo variants in RHOBTB2, an atypical Rho GTPase gene, cause epileptic encephalopathy. Human mutation. 39 (8), pp. 1070-1075. [Online].