Connection

ZEYNEP COBAN-AKDEMIR to Retina

This is a "connection" page, showing publications ZEYNEP COBAN-AKDEMIR has written about Retina.
Connection Strength

0.065
  1. De novo heterozygous variants in SLC30A7 are a candidate cause for Joubert syndrome. Am J Med Genet A. 2022 08; 188(8):2360-2366.
    View in: PubMed
    Score: 0.037
  2. Mutation in the intracellular chloride channel CLCC1 associated with autosomal recessive retinitis pigmentosa. PLoS Genet. 2018 08; 14(8):e1007504.
    View in: PubMed
    Score: 0.028
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.