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Author Report for: Del Val J

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    Title: Exome sequencing extends the phenotypic spectrum for ABHD12 mutations: from syndromic to nonsyndromic retinal degeneration
    Nishiguchi KM, Avila-Fernandez A, van Huet RA, Corton M, Perez-Carro R, Martin-Garrido E, Lopez-Molina MI, Blanco-Kelly F, Hoefsloot LH and Ayuso C <12 more author(s)>
    Ref: Ophthalmology, 121:1620, 2014 : PubMed

            


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