Publications
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Filters: Author is Xu, Mingchu and Keyword is Carrier Proteins [Clear All Filters]
Delineating the expanding phenotype associated with SCAPER gene mutation. Am J Med Genet A. 2019 ;179(8):1665-1671.
. Mutations in human IFT140 cause non-syndromic retinal degeneration. Hum Genet. 2015 ;134(10):1069-78.
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