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Novel de novo EEF1A2 missense mutations causing epilepsy and intellectual disability.
Lam WW, Millichap JJ, Soares DC, Chin R, McLellan A, FitzPatrick DR, Elmslie F, Lees MM, Schaefer GB; DDD study; Abbott CM. Lam WW, et al. Among authors: chin r. Mol Genet Genomic Med. 2016 Apr 3;4(4):465-74. doi: 10.1002/mgg3.219. eCollection 2016 Jul. Mol Genet Genomic Med. 2016. PMID: 27441201 Free PMC article.
Children's understanding of epilepsy: A qualitative study.
Harden J, Black R, Pickersgill M, Shetty J, McLellan A, Brand C, Small M, McDonnell J, Clarke L, Chin RF. Harden J, et al. Among authors: chin rf. Epilepsy Behav. 2021 Jul;120:107994. doi: 10.1016/j.yebeh.2021.107994. Epub 2021 May 5. Epilepsy Behav. 2021. PMID: 33964537 Free PMC article.
714 results