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Connection

RICHARD KELLERMAYER to Epilepsy

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This is a "connection" page, showing publications RICHARD KELLERMAYER has written about Epilepsy.
RICHARD KELLERMAYER
Connection Strength
0.009
Epilepsy
  1. Maternally inherited deafness and unusual phenotypic manifestations associated with A3243G mitochondrial DNA mutation. Pathol Oncol Res. 2005; 11(2):82-6.
    View in: PubMed
    Score: 0.009
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.