RINKI RATNA PRIYA to Adult
This is a "connection" page, showing publications RINKI RATNA PRIYA has written about Adult.
Connection Strength
0.013
-
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: 0.007
-
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.
Score: 0.006