Connection

RINKI RATNA PRIYA to Mutation

This is a "connection" page, showing publications RINKI RATNA PRIYA has written about Mutation.
Connection Strength

0.115
  1. Molecular Diagnosis of Inherited Retinal Diseases in Indigenous African Populations by Whole-Exome Sequencing. Invest Ophthalmol Vis Sci. 2016 11 01; 57(14):6374-6381.
    View in: PubMed
    Score: 0.104
  2. Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration. Hum Mol Genet. 2014 Nov 01; 23(21):5827-37.
    View in: PubMed
    Score: 0.011
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.