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Dravet syndrome with SCN1B gene mutation: A rare entity.
Mukherjee D, Mukherjee S, Niyogi P, Mahapatra M. Mukherjee D, et al. Neurol India. 2017 Jul-Aug;65(4):801-803. doi: 10.4103/neuroindia.NI_1115_15. Neurol India. 2017. PMID: 28681755 Free article.
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