Clinical characterization, linkage analysis, and PRPC8 mutation analysis of a family with autosomal dominant retinitis pigmentosa type 13 (RP13)
van Lith-Verhoeven, J.J.C., van der Velde-Visser, S.D., Sohocki, M.M., Deutman, A.F., Brink, H.M.A., Cremers, F.P.M., Hoyng, C.B.
Published in Ophthalmic genetics (2002)
Published in Ophthalmic genetics (2002)
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