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Missense mutation (Arg121Trp) in the Norrie disease gene associated with x-linked exudative vitreoretinopathy

S Fuchs1, U Kellner, H Wedemann

  • 1Institut für Humangenetik, Medizinische Universität, Lübeck, Germany.

Human Mutation
|January 1, 1995
PubMed
Abstract

No abstract available in PubMed .

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