RINKI RATNA PRIYA to Frameshift Mutation
This is a "connection" page, showing publications RINKI RATNA PRIYA has written about Frameshift Mutation.
Connection Strength
0.125
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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.
Score: 0.125