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Connection

Gil Shaulsky to Mutation, Missense

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This is a "connection" page, showing publications Gil Shaulsky has written about Mutation, Missense.
Gil Shaulsky
Connection Strength
0.101
Mutation, Missense
  1. A de novo loss-of-function GRIN2A mutation associated with childhood focal epilepsy and acquired epileptic aphasia. PLoS One. 2017; 12(2):e0170818.
    View in: PubMed
    Score: 0.101
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.