Publications by authors named "Justin Wilkin"

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Characterization of a Case of Pigmentary Retinopathy in Sanfilippo Syndrome Type IIIA Associated with Compound Heterozygous Mutations in the SGSH Gene.
Justin Wilkin, Natalie C Kerr, Kathryn W Byrd, Jewell C Ward, Alessandro Iannaccone

Ophthalmic Genetยท June 2016

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