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Filters: Keyword is Retinitis Pigmentosa and Author is Fu, Qing [Clear All Filters]
is mutated in a distinct type of Usher syndrome. J Med Genet. 2017 ;54(3):190-195.
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Next-generation sequencing-based molecular diagnosis of a Chinese patient cohort with autosomal recessive retinitis pigmentosa. Invest Ophthalmol Vis Sci. 2013 ;54(6):4158-66.
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