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Academic Journal

A new VCAN/versican splice acceptor site mutation in a French Wagner family associated with vascular and inflammatory ocular features.

Authors : Brézin AP; Université Paris-Descartes, Centre Cochin Ambulatoire d’Ophtalmologie, Assistance Publique Hôpitaux de Paris, France.; Nedelec B

Subjects: Mutation*; Neovascularization, Pathologic/Neovascularization, Pathologic/Neovascularization, Pathologic/*genetics ; Retinal Degeneration/Retinal Degeneration/Retinal Degeneration/*genetics Hyaloideoretinal degeneration of Wagner

Source: Molecular vision [Mol Vis] 2011; Vol. 17, pp. 1669-78. Date of Electronic Publication: 2011 Jun 22.Publisher: Molecular Vision Country of Publication: United States NLM ID: 9605351 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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