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Connection

RINKI RATNA PRIYA to Usher Syndromes

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This is a "connection" page, showing publications RINKI RATNA PRIYA has written about Usher Syndromes.
RINKI RATNA PRIYA
Connection Strength
0.033
Usher Syndromes
  1. Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss. Am J Hum Genet. 2016 09 01; 99(3):777-784.
    View in: PubMed
    Score: 0.033
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.