Export 4 results:
Filters: Author is Yuan, Zhisheng [Clear All Filters]
CEP78 is mutated in a distinct type of Usher syndrome. J Med Genet. 2016 ;..
Mutations in the Spliceosome Component CWC27 Cause Retinal Degeneration with or without Additional Developmental Anomalies. Am J Hum Genet. 2017 ;100(4):592-604..
The phenotypic variability of HK1-associated retinal dystrophy. Sci Rep. 2017 ;7(1):7051..