Connection

REBECCA LITTLEJOHN to Loss of Function Mutation

This is a "connection" page, showing publications REBECCA LITTLEJOHN has written about Loss of Function Mutation.
Connection Strength

0.210
  1. A cardiovascular, craniofacial, and neurodevelopmental disorder caused by loss-of-function variants in the eIF3 complex component genes EIF3A and EIF3B. Am J Hum Genet. 2025 11 06; 112(11):2625-2642.
    View in: PubMed
    Score: 0.210
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.