Connection

RUI CHEN to Point Mutation

This is a "connection" page, showing publications RUI CHEN has written about Point Mutation.
Connection Strength

0.435
  1. Rapid identification of heterozygous mutations in Drosophila melanogaster using genomic capture sequencing. Genome Res. 2010 Jul; 20(7):981-8.
    View in: PubMed
    Score: 0.304
  2. NMNAT1 E257K variant, associated with Leber Congenital Amaurosis (LCA9), causes a mild retinal degeneration phenotype. Exp Eye Res. 2018 08; 173:32-43.
    View in: PubMed
    Score: 0.131
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.