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Connection

ROHINI COORG to Mutation

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This is a "connection" page, showing publications ROHINI COORG has written about Mutation.
ROHINI COORG
Connection Strength
0.060
Mutation
  1. Nav1.2 channel mutations preventing fast inactivation lead to SCN2A encephalopathy. Brain. 2025 Jan 07; 148(1):212-226.
    View in: PubMed
    Score: 0.021
  2. Novel Genetic and Phenotypic Expansion in GOSR2-Related Progressive Myoclonus Epilepsy. Genes (Basel). 2023 09 25; 14(10).
    View in: PubMed
    Score: 0.020
  3. KCNA1 gain-of-function epileptic encephalopathy treated with 4-aminopyridine. Ann Clin Transl Neurol. 2023 04; 10(4):656-663.
    View in: PubMed
    Score: 0.019
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.