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Publication
Isolated and syndromic retinal dystrophy caused by biallelic mutations in RCBTB1, a gene implicated in ubiquitination
Journal Contribution - Journal Article
Journal: AMERICAN JOURNAL OF HUMAN GENETICS
ISSN: 0002-9297
Issue: 2
Volume: 99
Pages: 470 - 480
Publication year:2016
BOF-keylabel:yes
IOF-keylabel:yes
BOF-publication weight:10
CSS-citation score:2
Authors:International
Authors from:Higher Education
Accessibility:Open