IMEN CHAKCHOUK to Usher Syndromes
This is a "connection" page, showing publications IMEN CHAKCHOUK has written about Usher Syndromes.
Connection Strength
0.038
-
Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment. BMC Med Genet. 2018 07 20; 19(1):122.
Score: 0.038
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.