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Filters: Keyword is Homozygote and Author is Wang, Keqing [Clear All Filters]
is mutated in a distinct type of Usher syndrome. J Med Genet. 2017 ;54(3):190-195.
. A homozygous missense mutation in NEUROD1 is associated with nonsyndromic autosomal recessive retinitis pigmentosa. Invest Ophthalmol Vis Sci. 2014 ;56(1):150-5.
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