HIGHLIGHTS
- who: Andreea Nissenkorn and collaborators from the Sheba Medical Center, Tel HaShomer, Sackler School of Medicine, Tel Aviv University, Tel Aviv have published the paper: In vivo, in vitro and in silico correlations of four de novo SCN1A missense mutations, in the Journal: PLOS ONE | https://doi.org/10.1371/journal.pone [0211901]. February 8, 2019 of /1371/
- what: Interestingly, in contrast to de novo SCN1A mutations, which are the focus of this report, the clinical outcome of inherited SCN1A mutations varies even among kin, probably due to the influence of modifier genes . The authors . . .
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