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Connection

BRENDAN LEE to Loss of Function Mutation

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This is a "connection" page, showing publications BRENDAN LEE has written about Loss of Function Mutation.
BRENDAN LEE
Connection Strength
0.042
Loss of Function Mutation
  1. Heterozygous variants in SPTBN1 cause intellectual disability and autism. Am J Med Genet A. 2021 07; 185(7):2037-2045.
    View in: PubMed
    Score: 0.042
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.