Publications
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Filters: Author is Sui, Ruifang and Keyword is Consanguinity [Clear All Filters]
Isolated and Syndromic Retinal Dystrophy Caused by Biallelic Mutations in RCBTB1, a Gene Implicated in Ubiquitination. Am J Hum Genet. 2016 ;99(2):470-80.
. is mutated in a distinct type of Usher syndrome. J Med Genet. 2017 ;54(3):190-195.
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